- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT00845728
Exacerbation Study (INVIGORATE)
maanantai 16. syyskuuta 2013 päivittänyt: Novartis Pharmaceuticals
A Phase IIIb Multicenter, 52 Week Treatment, Randomized, Blinded, Double Dummy, Parallel Group Efficacy Study Comparing the Effect of Inhaled Indacaterol 150 µg o.d. vs Inhaled Tiotropium 18 µg o.d. on Lung Function, Rate of Exacerbations and Related Outcomes in Patients With COPD
This study compares indacaterol with tiotropium in terms of bronchodilation over 52 weeks
Tutkimuksen yleiskatsaus
Tila
Valmis
Interventio / Hoito
Opintotyyppi
Interventio
Ilmoittautuminen (Todellinen)
3439
Vaihe
- Vaihe 3
Yhteystiedot ja paikat
Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.
Opiskelupaikat
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Almelo, Alankomaat, 7609 PP
- Novartis Investigative Site
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Breda, Alankomaat, 4819 EV
- Novartis Investigative Site
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Eindhoven, Alankomaat, 5623 EJ
- Novartis Investigative Site
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Enschede, Alankomaat, 7513 ER
- Novartis Investigative Site
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Rotterdam, Alankomaat, 3045 PM
- Novartis Investigative Site
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Sneek, Alankomaat, 8601 ZK
- Novartis Investigative Site
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Zwolle, Alankomaat, 8011 JW
- Novartis Investigative Site
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Buenos Aires, Argentiina
- Novartis Investigative Site
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Buenos Aires, Argentiina, B1842DID
- Novartis Investigative Site
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Buenos Aires, Argentiina, C1122AAK
- Novartis Investigative Site
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Buenos Aires, Argentiina, C1125ABE
- Novartis Investigative Site
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Buenos Aires, Argentiina, 5000
- Novartis Investigative Site
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Buenos Aires, Argentiina, C1426ABP
- Novartis Investigative Site
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Buenos aires, Argentiina, C1221ADC
- Novartis Investigative Site
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Mendoza, Argentiina, M5500CCG
- Novartis Investigative Site
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Buenos Aires
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Capital Federal, Buenos Aires, Argentiina, C1424BSF
- Novartis Investigative Site
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Mar del Plata, Buenos Aires, Argentiina, 7600
- Novartis Investigative Site
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Pilar, Buenos Aires, Argentiina, B1629AHJ
- Novartis Investigative Site
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Santa Fe
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Rosario, Santa Fe, Argentiina, C2000DSR
- Novartis Investigative Site
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Rosario, Santa Fe, Argentiina, S2000AYW
- Novartis Investigative Site
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Tucuman
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San Miguel de Tucuman, Tucuman, Argentiina, 4000
- Novartis Investigative Site
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Tauranga, New Zealand, Australia, 3001
- Novartis Investigative Site
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New South Wales
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Bankstown, New South Wales, Australia, 2200
- Novartis Investigative Site
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South Australia
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Adelaide, South Australia, Australia, 5000
- Novartis Investigative Site
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Daw Park, South Australia, Australia, 5041
- Novartis Investigative Site
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Victoria
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Heidelberg, Victoria, Australia, 3084
- Novartis Investigative Site
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Parkville, Victoria, Australia, 3050
- Novartis Investigative Site
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Western Australia
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Nedlands, Western Australia, Australia, 6009
- Novartis Investigative Site
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Aalst, Belgia, 9300
- Novartis Investigative Site
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Antwerpen, Belgia, 2020
- Novartis Investigative Site
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Bruxelles, Belgia, 1200
- Novartis Investigative Site
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Bruxelles, Belgia, 1000
- Novartis Investigative Site
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Duffel, Belgia, 2570
- Novartis Investigative Site
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Eupen, Belgia, 4700
- Novartis Investigative Site
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Framerie, Belgia, 7080
- Novartis Investigative Site
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Geraardsbergen, Belgia, 9500
- Novartis Investigative Site
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Gilly, Belgia, 6060
- Novartis Investigative Site
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Godinne, Belgia, 5530
- Novartis Investigative Site
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Gozée, Belgia, 6534
- Novartis Investigative Site
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Herentals, Belgia, 2200
- Novartis Investigative Site
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Jambes, Belgia, 5100
- Novartis Investigative Site
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Jette, Belgia, 1090
- Novartis Investigative Site
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Kortrijk, Belgia, 8500
- Novartis Investigative Site
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Leuven, Belgia, 3000
- Novartis Investigative Site
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Liege, Belgia, 4000
- Novartis Investigative Site
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Liège, Belgia, 4000
- Novartis Investigative Site
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Malmedy, Belgia, 4960
- Novartis Investigative Site
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Menen, Belgia, 8930
- Novartis Investigative Site
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Montigny-le-tilleul, Belgia, 6110
- Novartis Investigative Site
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Namur, Belgia, 5000
- Novartis Investigative Site
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Oostende, Belgia, 8400
- Novartis Investigative Site
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Turnhout, Belgia, 2300
- Novartis Investigative Site
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GO
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Goiania, GO, Brasilia, 74605-050
- Novartis Investigative Site
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MG
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Juiz de Fora, MG, Brasilia, 36036-110
- Novartis Investigative Site
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RJ
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Rio de Janeiro, RJ, Brasilia, 22271-110
- Novartis Investigative Site
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RS
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Caxias do Sul, RS, Brasilia, 95070-560
- Novartis Investigative Site
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Porto Alegre, RS, Brasilia, 90020-090
- Novartis Investigative Site
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Porto Alegre, RS, Brasilia, 90610-000
- Novartis Investigative Site
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Porto Alegre, RS, Brasilia, 90880-480
- Novartis Investigative Site
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SP
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São Paulo, SP, Brasilia, 04023-062
- Novartis Investigative Site
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San Francisco de Asís, Costa Rica
- Novartis Investigative Site
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San Jose, Costa Rica
- Novartis Investigative Site
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Madrid, Espanja, 28007
- Novartis Investigative Site
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Madrid, Espanja, 28040
- Novartis Investigative Site
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Andalucia
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Jerez de La Frontera, Andalucia, Espanja, 11407
- Novartis Investigative Site
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Malaga, Andalucia, Espanja, 29010
- Novartis Investigative Site
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Sanlúcar de Barrameda, Andalucia, Espanja, 11540
- Novartis Investigative Site
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Sevilla, Andalucia, Espanja, 41009
- Novartis Investigative Site
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Asturias
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Gijon, Asturias, Espanja, 33290
- Novartis Investigative Site
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Castilla la Mancha
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Illescas, Castilla la Mancha, Espanja, 45200
- Novartis Investigative Site
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Castilla y Leon
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Valladolid, Castilla y Leon, Espanja, 47011
- Novartis Investigative Site
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Cataluña
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Barcelona, Cataluña, Espanja, 08003
- Novartis Investigative Site
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Barcelona, Cataluña, Espanja, 08041
- Novartis Investigative Site
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Barcelona, Cataluña, Espanja, 08036
- Novartis Investigative Site
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Salt, Cataluña, Espanja, 17190
- Novartis Investigative Site
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Sant Boi de Llobregat, Cataluña, Espanja, 08830
- Novartis Investigative Site
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Terrassa, Cataluña, Espanja, 08221
- Novartis Investigative Site
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Vic, Cataluña, Espanja, 08500
- Novartis Investigative Site
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Comunidad Valenciana
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Alicante, Comunidad Valenciana, Espanja, 03114
- Novartis Investigative Site
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Alzira, Comunidad Valenciana, Espanja, 46600
- Novartis Investigative Site
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Requena, Comunidad Valenciana, Espanja, 46340
- Novartis Investigative Site
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Extremadura
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Caceres, Extremadura, Espanja, 10003
- Novartis Investigative Site
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Mérida, Extremadura, Espanja, 06800
- Novartis Investigative Site
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Plasencia, Extremadura, Espanja, 10600
- Novartis Investigative Site
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Galicia
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La Coruna, Galicia, Espanja, 15006
- Novartis Investigative Site
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Lugo, Galicia, Espanja, 27003
- Novartis Investigative Site
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Santiago de Compostela, Galicia, Espanja, 15706
- Novartis Investigative Site
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Madrid
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Pozuelo de Alarcón, Madrid, Espanja, 28223
- Novartis Investigative Site
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Bloemfontein, Etelä-Afrikka, 9301
- Novartis Investigative Site
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Bloemfontein, Etelä-Afrikka, 9317
- Novartis Investigative Site
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Cape Town, Etelä-Afrikka, 8001
- Novartis Investigative Site
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Durban, Etelä-Afrikka, 4001
- Novartis Investigative Site
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Quezon City, Filippiinit, 1100
- Novartis Investigative Site
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Quezon City, Filippiinit, 1101
- Novartis Investigative Site
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Metro Manila
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Quezon City, Metro Manila, Filippiinit, 1109
- Novartis Investigative Site
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Quezon City, Metro Manila, Filippiinit, 1104
- Novartis Investigative Site
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Nagpur - Maharashtra, Intia, 440012
- Novartis Investigative Site
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Nagpur - Maharastra, Intia, 400 012
- Novartis Investigative Site
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Panjim, Intia, 403002
- Novartis Investigative Site
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Andhra Pradesh
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Hyderabad, Andhra Pradesh, Intia, 500004
- Novartis Investigative Site
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Hyderabad, Andhra Pradesh, Intia, 500012
- Novartis Investigative Site
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Delhi
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New Delhi, Delhi, Intia, 110029
- Novartis Investigative Site
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Gujrat
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Ahmedabad, Gujrat, Intia, 380009
- Novartis Investigative Site
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Gujrat-India
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Ahmedabad, Gujrat-India, Intia, 380054
- Novartis Investigative Site
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Karnataka
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Bangalore, Karnataka, Intia, 560002
- Novartis Investigative Site
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Bangalore, Karnataka, Intia, 560 002
- Novartis Investigative Site
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Mangalore, Karnataka, Intia, 575001
- Novartis Investigative Site
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Kerala
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Calicut, Kerala, Intia, 673008
- Novartis Investigative Site
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Trivandrum, Kerala, Intia, 695011
- Novartis Investigative Site
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Madhya Pradesh
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Indore, Madhya Pradesh, Intia, 452001
- Novartis Investigative Site
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New Delhi
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Noida, New Delhi, Intia, 201301
- Novartis Investigative Site
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Rajasthan
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Jaipur, Rajasthan, Intia, 302023
- Novartis Investigative Site
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Tamil Nadu
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Coimbatore, Tamil Nadu, Intia, 641 002
- Novartis Investigative Site
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Vellore, Tamil Nadu, Intia, 632004
- Novartis Investigative Site
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Reykjavik, Islanti, IS-109
- Novartis Investigative Site
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Ashkelon, Israel, 78278
- Novartis Investigative Site
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Jerusalem, Israel, 91120
- Novartis Investigative Site
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Ramat Gan, Israel, 52621
- Novartis Investigative Site
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Rehovot, Israel, 76100
- Novartis Investigative Site
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Tel-Aviv, Israel, 64239
- Novartis Investigative Site
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Napoli, Italia, 80131
- Novartis Investigative Site
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Pisa, Italia, 56124
- Novartis Investigative Site
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BA
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Acquaviva delle Fonti, BA, Italia, 70021
- Novartis Investigative Site
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Bari, BA, Italia, 70124
- Novartis Investigative Site
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BG
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Bergamo, BG, Italia, 24128
- Novartis Investigative Site
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BS
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Brescia, BS, Italia, 25127
- Novartis Investigative Site
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CZ
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Catanzaro, CZ, Italia, 88100
- Novartis Investigative Site
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FE
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Cona, FE, Italia, 44100
- Novartis Investigative Site
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FR
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Cassino, FR, Italia, 03043
- Novartis Investigative Site
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GE
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Genova, GE, Italia, 16132
- Novartis Investigative Site
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MI
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Milano, MI, Italia, 20142
- Novartis Investigative Site
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Milano, MI, Italia, 20126
- Novartis Investigative Site
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Milano, MI, Italia, 20157
- Novartis Investigative Site
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MO
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Modena, MO, Italia, 41100
- Novartis Investigative Site
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PA
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Palermo, PA, Italia, 90146
- Novartis Investigative Site
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PN
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Pordenone, PN, Italia, 33170
- Novartis Investigative Site
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PO
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Prato, PO, Italia, 59100
- Novartis Investigative Site
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PR
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Parma, PR, Italia, 43100
- Novartis Investigative Site
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RM
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Roma, RM, Italia, 00168
- Novartis Investigative Site
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Roma, RM, Italia, 00161
- Novartis Investigative Site
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Roma, RM, Italia, 00133
- Novartis Investigative Site
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Roma, RM, Italia, 00163
- Novartis Investigative Site
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SA
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Cava Dei Tirreni, SA, Italia, 84013
- Novartis Investigative Site
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SI
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Siena, SI, Italia, 53100
- Novartis Investigative Site
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TE
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Teramo, TE, Italia, 64100
- Novartis Investigative Site
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TO
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Orbassano, TO, Italia, 10043
- Novartis Investigative Site
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TS
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Trieste, TS, Italia, 34149
- Novartis Investigative Site
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VA
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Cuasso al Monte, VA, Italia, 21050
- Novartis Investigative Site
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VR
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Verona, VR, Italia, 37126
- Novartis Investigative Site
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Feldbach, Itävalta, 8330
- Novartis Investigative Site
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Grieskirchen, Itävalta, 4710
- Novartis Investigative Site
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Gänserndorf, Itävalta, 2230
- Novartis Investigative Site
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Hallein, Itävalta, 5400
- Novartis Investigative Site
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Linz, Itävalta, 4020
- Novartis Investigative Site
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Perg, Itävalta, 4320
- Novartis Investigative Site
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Zwettl, Itävalta, 3910
- Novartis Investigative Site
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Alberta
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Calgary, Alberta, Kanada, T2N 4N1
- Novartis Investigative Site
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Calgary, Alberta, Kanada, T2V 1P9
- Novartis Investigative Site
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Edmonton, Alberta, Kanada, T6G 2B7
- Novartis Investigative Site
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British Columbia
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Kelowna, British Columbia, Kanada, V1Y 1E4
- Novartis Investigative Site
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Vancouver, British Columbia, Kanada, V5Z 3J5
- Novartis Investigative Site
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Manitoba
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Winnipeg, Manitoba, Kanada, R3C 0N2
- Novartis Investigative Site
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New Brunswick
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Moncton, New Brunswick, Kanada, E1G 1A7
- Novartis Investigative Site
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Ontario
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Burlington, Ontario, Kanada, L7N 3V2
- Novartis Investigative Site
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Mississauga, Ontario, Kanada, L5B 4A9
- Novartis Investigative Site
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Newmarket, Ontario, Kanada, L3Y 5G8
- Novartis Investigative Site
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Ottawa, Ontario, Kanada, K1Y 4G2
- Novartis Investigative Site
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Toronto, Ontario, Kanada, M6H 3M2
- Novartis Investigative Site
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Toronto, Ontario, Kanada, M5T 3A9
- Novartis Investigative Site
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Toronto, Ontario, Kanada, M5G1N8
- Novartis Investigative Site
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Quebec
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Montreal, Quebec, Kanada, H2L 4M1
- Novartis Investigative Site
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Montreal, Quebec, Kanada, H4J 1C5
- Novartis Investigative Site
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Montreal, Quebec, Kanada, H2L 2W5
- Novartis Investigative Site
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Montreal, Quebec, Kanada, H2X 2P4
- Novartis Investigative Site
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Sainte-Foy, Quebec, Kanada, G1V 4G5
- Novartis Investigative Site
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Sherbrooke, Quebec, Kanada, J1H 4J6
- Novartis Investigative Site
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Beijing, Kiina, 100020
- Novartis Investigative Site
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Beijing, Kiina, 100034
- Novartis Investigative Site
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Chongqing, Kiina, 400037
- Novartis Investigative Site
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Shanghai, Kiina, 200025
- Novartis Investigative Site
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Shen Yang, Kiina, 110001
- Novartis Investigative Site
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Hebei
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Shijiazhuang, Hebei, Kiina, 050000
- Novartis Investigative Site
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Hunan
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Changsha, Hunan, Kiina, 410003
- Novartis Investigative Site
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Changsha City, Hunan, Kiina, 410011
- Novartis Investigative Site
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Liaoning
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Shengyang, Liaoning, Kiina, 110016
- Novartis Investigative Site
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Shanxi
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Xi'an, Shanxi, Kiina, 710032
- Novartis Investigative Site
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Xi'an, Shanxi, Kiina, 710061
- Novartis Investigative Site
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Barranquilla, Kolumbia
- Novartis Investigative Site
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Bogotá, Kolumbia
- Novartis Investigative Site
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Medellín, Kolumbia
- Novartis Investigative Site
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Riga, Latvia, 1002
- Novartis Investigative Site
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LV
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Riga, LV, Latvia, LV-1038
- Novartis Investigative Site
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Kaunas, Liettua, 44320
- Novartis Investigative Site
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Klaipeda, Liettua, LT-92231
- Novartis Investigative Site
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Siauliai, Liettua, LT-76231
- Novartis Investigative Site
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Utena, Liettua, LT-28151
- Novartis Investigative Site
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Vilnius, Liettua, LT-08661
- Novartis Investigative Site
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San Luis Potosí, Meksiko, 78218
- Novartis Investigative Site
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Hidalgo
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Pachuca, Hidalgo, Meksiko, 42090
- Novartis Investigative Site
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Jalisco
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Guadalajara, Jalisco, Meksiko, 44100
- Novartis Investigative Site
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Guadalajara, Jalisco, Meksiko, 44280
- Novartis Investigative Site
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Nuevo León
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Monterrey, Nuevo León, Meksiko, 64450
- Novartis Investigative Site
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Lima
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Cercado de Lima, Lima, Peru, 01
- Novartis Investigative Site
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Jesus Maria, Lima, Peru, 11
- Novartis Investigative Site
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La Victoria, Lima, Peru, 13
- Novartis Investigative Site
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Miraflores, Lima, Peru, 18
- Novartis Investigative Site
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San Borja, Lima, Peru, 41
- Novartis Investigative Site
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San Isidro, Lima, Peru, 27
- Novartis Investigative Site
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San Martin de Porres, Lima, Peru, 31
- Novartis Investigative Site
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San Miguel, Lima, Peru, 32
- Novartis Investigative Site
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Santiago de Surco, Lima, Peru, 33
- Novartis Investigative Site
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Amadora, Portugali, 2720-276
- Novartis Investigative Site
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Coimbra, Portugali, 3000-075
- Novartis Investigative Site
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Coimbra, Portugali, 3041-853
- Novartis Investigative Site
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Lisboa, Portugali, 1649-035
- Novartis Investigative Site
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Lisboa, Portugali, 1169-024
- Novartis Investigative Site
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Lisboa, Portugali, 1769-001
- Novartis Investigative Site
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Porto, Portugali, 4200-319
- Novartis Investigative Site
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Gdansk, Puola, 80-169
- Novartis Investigative Site
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Gdansk, Puola, 80-847
- Novartis Investigative Site
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Katowice, Puola, 40-752
- Novartis Investigative Site
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Krakow, Puola, 31-159
- Novartis Investigative Site
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Krakow, Puola, 31-202
- Novartis Investigative Site
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Krakow, Puola, 31-455
- Novartis Investigative Site
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Warszawa, Puola, 02-341
- Novartis Investigative Site
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Warszawa, Puola, 01-138
- Novartis Investigative Site
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Wroclaw, Puola, 50-044
- Novartis Investigative Site
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Beuvry, Ranska, 62660
- Novartis Investigative Site
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Bourges, Ranska, 18000
- Novartis Investigative Site
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Ferolles-Attily, Ranska, 77150
- Novartis Investigative Site
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Lyon cedex 04, Ranska, 69317
- Novartis Investigative Site
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Montpellier, Ranska, 34059
- Novartis Investigative Site
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Nantes, Ranska, 44000
- Novartis Investigative Site
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Nice Cedex 1, Ranska, 06602
- Novartis Investigative Site
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Ollioules Cedex, Ranska, 83192
- Novartis Investigative Site
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Paris, Ranska, 75006
- Novartis Investigative Site
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Perpignan Cedex, Ranska, 66025
- Novartis Investigative Site
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Pessac, Ranska, 33604
- Novartis Investigative Site
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Reims, Ranska, 51092
- Novartis Investigative Site
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St Michel, Ranska, 16470
- Novartis Investigative Site
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Vandoeuvre les Nancy, Ranska, 54511
- Novartis Investigative Site
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Bucharest, Romania, 060011
- Novartis Investigative Site
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Cluj-Napoca, Romania, 400371
- Novartis Investigative Site
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District 3
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Bucharest, District 3, Romania, 030303
- Novartis Investigative Site
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Jud. Brasov
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Brasov, Jud. Brasov, Romania, 500118
- Novartis Investigative Site
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Jud. Constanta
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Constanta, Jud. Constanta, Romania, 900002
- Novartis Investigative Site
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Jud. Iasi
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Iasi, Jud. Iasi, Romania, 700115
- Novartis Investigative Site
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Göteborg, Ruotsi, 413 45
- Novartis Investigative Site
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Göteborg, Ruotsi, 412 63
- Novartis Investigative Site
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Luleå, Ruotsi, SE-971 80
- Novartis Investigative Site
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Lund, Ruotsi, SE-221 85
- Novartis Investigative Site
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Malmö, Ruotsi, 205 02
- Novartis Investigative Site
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Skellefteå, Ruotsi, SE 931 32
- Novartis Investigative Site
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Stockholm, Ruotsi, S-171 76
- Novartis Investigative Site
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Sundsvall, Ruotsi, 851 86
- Novartis Investigative Site
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Bad Woerishofen, Saksa, 86825
- Novartis Investigative Site
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Berlin, Saksa, 12043
- Novartis Investigative Site
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Berlin, Saksa, 12687
- Novartis Investigative Site
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Berlin, Saksa, 13086
- Novartis Investigative Site
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Berlin, Saksa, 10367
- Novartis Investigative Site
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Berlin, Saksa, 14050
- Novartis Investigative Site
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Berlin, Saksa, 10969
- Novartis Investigative Site
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Berlin, Saksa, 13581
- Novartis Investigative Site
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Berlin, Saksa, 13057
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Berlin, Saksa, 13507
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Bonn, Saksa, 53119
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Bonn, Saksa, 53123
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Borstel, Saksa, 23845
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Dachau, Saksa, 85221
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Euskirchen, Saksa, 53879
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Frankfurt, Saksa, 60596
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Güstrow, Saksa, 18273
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Hamburg, Saksa, 20354
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Hamburg, Saksa, 20357
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Hamburg, Saksa, 22299
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Hamburg, Saksa, 22305
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Hoyerswerda, Saksa, 02977
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Landsberg, Saksa, 86899
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Leipzig, Saksa, 04207
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Muenchen, Saksa, 80331
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Muenchen, Saksa, 80539
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Muenchen, Saksa, 81677
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Muenchen, Saksa, 81243
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München, Saksa, 80335
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Neu-Ulm, Saksa, 89231
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Neuss, Saksa, 41462
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Oranienburg, Saksa, 16515
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Radebeul, Saksa, 01445
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Ratingen, Saksa, 40878
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Rüdersdorf, Saksa, 15562
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Teterow, Saksa, 17166
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Ulm, Saksa, 89081
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Wedel, Saksa, 22880
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Witten, Saksa, 58452
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Bratislava, Slovakia, 826 06
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Lucenec, Slovakia, 984 39
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Nove Zamky, Slovakia, 940 01
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Poprad, Slovakia, 058 01
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Slovak Republic
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Bratislava, Slovak Republic, Slovakia, 821 06
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Bern, Sveitsi, 3013
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Thun, Sveitsi, 3600
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Zuerich, Sveitsi, 8032
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ZH
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Taichung, Taiwan, 40447
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Taichung, Taiwan, 40705
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Taipei, Taiwan, 10002
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Taipei, Taiwan, 110
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Taipei County, Taiwan
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Aalborg, Tanska, DK-9100
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Copenhagen NV, Tanska, DK-2400
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Hellerup, Tanska, DK-2900
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Helsingor, Tanska, DK-3000
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Hvidovre, Tanska, DK-2650
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Odense C, Tanska, DK-5000
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Århus, Tanska, DK-8000
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Bangkok, Thaimaa, 10700
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Chiang Mai, Thaimaa, 50200
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Songkla, Thaimaa, 90110
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Ankara, Turkki, 06100
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Canakkale, Turkki, 17100
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Diskapi / Ankara, Turkki, 06110
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Emek / Ankara, Turkki, 06510
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Gaziantep, Turkki, 27070
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Isparta, Turkki, 32100
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Istanbul, Turkki
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Beroun, Tšekin tasavalta
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Karlovy Vary, Tšekin tasavalta, 360 66
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Karlovy Vary, Tšekin tasavalta, 360 06
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Kurim, Tšekin tasavalta, 66434
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CZE
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Kyjov, CZE, Tšekin tasavalta, 697 70
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Valencia, Estado Carabobo, Venezuela, 2005
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Barquisimeto, Estado Lara, Venezuela, 3002
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Chelyabinsk, Venäjän federaatio, 454021
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Ekaterinburg, Venäjän federaatio, 620109
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Ekaterinburg, Venäjän federaatio, 620219
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Moscow, Venäjän federaatio, 121359
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Moscow, Venäjän federaatio, 105229
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Moscow, Venäjän federaatio, 119992
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Moscow, Venäjän federaatio, 115280
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Moscow, Venäjän federaatio, 105077
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Moscow, Venäjän federaatio, 115446
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Moscow, Venäjän federaatio, 121609
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Samara, Venäjän federaatio, 443079
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Rakvere, Viro, 44310
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England
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Swansea, England, Yhdistynyt kuningaskunta, SA6 6NL
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Surrey
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Ash Vale, Surrey, Yhdistynyt kuningaskunta, GU12 5BA
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West Sussex
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Osallistumiskriteerit
Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.
Kelpoisuusvaatimukset
Opintokelpoiset iät
40 vuotta ja vanhemmat (Aikuinen, Vanhempi Aikuinen)
Hyväksyy terveitä vapaaehtoisia
Ei
Sukupuolet, jotka voivat opiskella
Kaikki
Kuvaus
Inclusion Criteria:
- Male and female adults aged ≥40 years, who have signed an Informed Consent form prior to initiation of any study-related procedure
Patients diagnosed with COPD at age 40 and over and with a current diagnosis of severe COPD and including:
- Smoking history of at least 10 pack years, both current and ex-smokers are eligible
- A documented history of at least 1 moderate or severe exacerbation in the previous 12 months
Exclusion Criteria:
- Patients who have received systemic corticosteroids and/or antibiotics for a COPD exacerbation in the 6 weeks prior to screening or during the run-in period
- Patients who have had a respiratory tract infection within 6 weeks prior to screening
- Patients with concomitant pulmonary disease
- Patients with a history of asthma
- Patients with diabetes Type I or uncontrolled diabetes Type II
- Any patient with lung cancer or a history of lung cancer
- Patients with a history of certain cardiovascular comorbid conditions
Other protocol-defined inclusion/exclusion criteria may apply
Opintosuunnitelma
Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Nelinkertaistaa
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: Indacaterol
Indacaterol 150 µg o.d.
delivered via single-dose dry powder inhaler (SDDPI)
|
Indacaterol 150 µg o.d.
delivered via SDDPI
|
|
Active Comparator: Tiotropium
Tiotropium 18 µg o.d.
delivered via the handihaler®
|
Tiotropium 18 µg o.d.
delivered via handihaler®
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Trough Forced Expiratory Volume in 1 Second (FEV1).
Aikaikkuna: 12 weeks
|
The primary objective of the study was to demonstrate the non-inferiority of indacaterol vs. tiotropium with respect to 24 hour post dose (trough) FEV1 after 12 weeks of treatment in patients with severe COPD.
Trough FEV1 was defined as the average of the 23 hours 10 min and the 23 hours 45 min post dose values.
Trough FEV1 was analyzed using a mixed model for the PPS-S.
The model contained treatment as a fixed effect with the baseline FEV1, FEV1 prior to inhalation and FEV1 15 min post-inhalation of salbutamol/albuterol (components of SABA reversibility at Visit 2), FEV1 prior to inhalation and FEV1 60 min post-inhalation of ipratropium (components of anti-cholinergic reversibility at Visit 3) as covariates.
Smoking history (current or ex-smoker) was included as a factor in the model.
|
12 weeks
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Rate of COPD Exacerbations
Aikaikkuna: 52 weeks
|
COPD exacerbations were defined as :Worsening of 2 or more major symptoms for at least 2 consecutive days: dyspnea; sputum volume; suputum purulence AND requiring treatment with systemic corticosteroids and/or antibiotics OR Worsening of any 1 major symptom together with any 1 of the following minor symptoms for at least 2 consecutive days: Sore throat; colds; fever without other cause; increased cough; increase wheeze AND requiring treatment with systemic glucocorticosteroids and/or antibiotics.
The rate was analyzed using a linear model assuming a negative binomial distribution for the PPS-E.
The time at risk for a patient was defined as the length of time the patient was in the study and the log(length of time in the study) was used as the offset variable in the model.
|
52 weeks
|
Yhteistyökumppanit ja tutkijat
Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.
Sponsori
Julkaisuja ja hyödyllisiä linkkejä
Tutkimusta koskevien tietojen syöttämisestä vastaava henkilö toimittaa nämä julkaisut vapaaehtoisesti. Nämä voivat koskea mitä tahansa tutkimukseen liittyvää.
Opintojen ennätyspäivät
Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan julkisella verkkosivustolla.
Opi tärkeimmät päivämäärät
Opiskelun aloitus
Sunnuntai 1. maaliskuuta 2009
Ensisijainen valmistuminen (Todellinen)
Sunnuntai 1. heinäkuuta 2012
Opintojen valmistuminen (Todellinen)
Sunnuntai 1. heinäkuuta 2012
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Sunnuntai 15. helmikuuta 2009
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Tiistai 17. helmikuuta 2009
Ensimmäinen Lähetetty (Arvio)
Keskiviikko 18. helmikuuta 2009
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Arvio)
Tiistai 19. marraskuuta 2013
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Maanantai 16. syyskuuta 2013
Viimeksi vahvistettu
Sunnuntai 1. syyskuuta 2013
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
- Hengityselinten sairaudet
- Keuhkosairaudet
- Keuhkosairaudet, obstruktiiviset
- Keuhkosairaus, krooninen obstruktiivinen
- Huumeiden fysiologiset vaikutukset
- Neurotransmitterit
- Farmakologisen vaikutuksen molekyylimekanismit
- Parasympatolyytit
- Autonomiset agentit
- Ääreishermoston aineet
- Kolinergiset antagonistit
- Kolinergiset aineet
- Keuhkoputkia laajentavat aineet
- Astmaattiset aineet
- Hengityselinten aineet
- Tiotropiumbromidi
Muut tutkimustunnusnumerot
- CQAB149B2348
- 2008-007944-33
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .