- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01400971
Eine Beobachtungsstudie zum Verständnis der Herausforderungen im Zusammenhang mit dem Fortschreiten der Insulintherapie bei Typ-2-Diabetes (MOSAIc)
25. Februar 2020 aktualisiert von: Eli Lilly and Company
Eine multinationale Beobachtungsstudie zur Bewertung des Insulingebrauchs: Verständnis der Herausforderungen im Zusammenhang mit dem Fortschreiten der Therapie - Die MOSAIC-Typ-2-Diabetes-Studie
Der Zweck dieser Studie ist es, spezifische patienten-, arzt- und gesundheitssystembezogene Faktoren zu identifizieren, die mit dem Übergang zu einem intensiveren Regime von der anfänglichen Insulintherapie für Patienten mit Typ-2-Diabetes verbunden sind.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Studientyp
Beobachtungs
Einschreibung (Tatsächlich)
4299
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Buenos Aires, Argentinien, CBA 1419
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Corrientes, Argentinien, 3400
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Mendoza, Argentinien, 5500
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Parana, Argentinien, 3100
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Rosario, Argentinien, S2000DSZ
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San Juan, Argentinien, 5400
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Campina Grande Do Sul, Brasilien, 83430-000
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Caxias Do Sul, Brasilien, 95070560
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Fortaleza, Brasilien, 60430-370
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Santa Maria, Brasilien, 97015-530
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Setor Oeste/Goiania, Brasilien, 74100-120
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São Paulo, Brasilien, 04020-041
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Tatui, Brasilien, 18270-170
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Beijing, China, 100101
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Changchun City, China, 130041
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Chongqing, China
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Guang Zhou, China, 510080
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Shijiazhuang, China, 50000
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Xi'An, China, 710061
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Bosenheim, Deutschland, 55545
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Dresden, Deutschland, 01307
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Essen, Deutschland, 45359
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Hamburg, Deutschland, 22415
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Hohenmölsen, Deutschland, 06679
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Kamp-Lintfort, Deutschland, 47475
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Köln, Deutschland, 51069
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Lambrecht, Deutschland, 67466
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Schramberg, Deutschland, 78713
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Speyer, Deutschland, 67346
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Ahmedabad, Indien, 380007
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Ahmedabad, Gujarat, Indien, 380009
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Bangalore, Indien, 560054
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Belgaum, Indien, 590001
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Hyderabaad, Indien, 500033
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Jaipur, Indien, 302020
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Kormangala, Indien, 560034
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Mangalore, Indien, 575001
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Mumbai, Indien, 400053
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Mysore, Indien, 570023
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Nagpur, Indien, 440025
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New Delhi, Indien, 110070
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Pune, Indien, 411035
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Beer Sheva, Israel, 84350
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Beer Yaakov, Israel, 70300
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Dimona, Israel, 68000
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Givataim, Israel, 53488
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Netanya, Israel, 42470
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Petach Tikwa, Israel, 49582
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Rishon Le Zion, Israel, 75650
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Safed, Israel, 13110
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Acquaviva Delle Fonti, Italien, 70021
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Ancona, Italien, 60110
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Foggia, Italien, 71100
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Lucca, Italien, 55100
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Napoli, Italien, 80131
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Parma, Italien, 43100
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Pavia, Italien, 27100
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Rome, Italien, 00168
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San Giovanni Rotondo, Italien, 71013
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Siena, Italien, 53100
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Kanagawa, Japan, 242-0004
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Kanagawa-Ken, Japan, 232-0071
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Alberta
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Edmonton, Alberta, Kanada, T5A 4L8
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Spruce Grove, Alberta, Kanada, T7X 2V2
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Manitoba
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Winnipeg, Manitoba, Kanada, R3C 0N2
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Newfoundland and Labrador
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St. John'S, Newfoundland and Labrador, Kanada, A1A3R5
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Ontario
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Burlington, Ontario, Kanada, L7M 4Y1
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London, Ontario, Kanada, N6A 5G6
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Smiths Falls, Ontario, Kanada, K7A 4W8
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Quebec
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Gatineau, Quebec, Kanada, J8V 2P5
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Montreal, Quebec, Kanada, H3N 1S4
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Sherbrooke, Quebec, Kanada, J1G 1B8
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Daegu, Korea, Republik von, 705-717
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Daejeon, Korea, Republik von, 301-721
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Gangwon-Do, Korea, Republik von, 200-722
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Goyang-Si, Korea, Republik von, 412-270
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Jeju Special Self-Governing Pr, Korea, Republik von, 690-767
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Sungnam-Si, Korea, Republik von, 463-712
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Aguascalientes, Mexiko, 20217
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Durango, Mexiko, 34080
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Guadalajara, Mexiko, 44680
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Huixquilucan, Mexiko, 52763
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Mexico City, Mexiko, 11850
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Zapopan, Mexiko, 45200
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Bayamon, Puerto Rico, 00956
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Carolina, Puerto Rico, 00983
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Loiza, Puerto Rico, 772
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Rio Grande, Puerto Rico, 00745
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Rio Piedras, Puerto Rico, 00921
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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San Juan, Puerto Rico, 00920
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Toa Baja, Puerto Rico, 00949
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Villa Fontana, Puerto Rico, 00983
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Moscow, Russische Föderation, 117997
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Nizhniy Novgorod, Russische Föderation, 603126
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Rostov-On-Don, Russische Föderation, 344022
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Saint Petersburg, Russische Föderation, 194358
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tomsk, Russische Föderation, 634050
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Vsevolozhsk, Russische Föderation, 188640
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Yaroslavl, Russische Föderation, 150010
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Dammam, Saudi-Arabien, 31412
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Makkah, Saudi-Arabien, 21955
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Riyadh, Saudi-Arabien, 245
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Taif, Saudi-Arabien, 21944
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Barcelona, Spanien, 8025
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Gerena, Spanien
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La Roca Del Valles, Spanien, 8430
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Madrid, Spanien, 28034
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Sevilla, Spanien, 41009
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Vic, Spanien, 08500
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Ankara, Truthahn, 6560
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Canakkale, Truthahn, 06310
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Diyarbakir, Truthahn, 21280
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Gaziantep, Truthahn, 27310
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Istanbul, Truthahn, 34865
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Izmir, Truthahn
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kahramanmaras, Truthahn, 46050
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kirikkale, Truthahn, 71450
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Abu Dhabi, Vereinigte Arabische Emirate
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Al Ain, Vereinigte Arabische Emirate
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Dubai, Vereinigte Arabische Emirate, 9115
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sharjah, Vereinigte Arabische Emirate
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Arkansas
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Little Rock, Arkansas, Vereinigte Staaten, 72204
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Florida
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Orlando, Florida, Vereinigte Staaten, 32806
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wellington, Florida, Vereinigte Staaten, 33414
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Georgia
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Canton, Georgia, Vereinigte Staaten, 30114
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Illinois
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Crystal Lake, Illinois, Vereinigte Staaten, 60012
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Nebraska
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North Platte, Nebraska, Vereinigte Staaten, 69101
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Nevada
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Reno, Nevada, Vereinigte Staaten, 89511
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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North Carolina
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Burlington, North Carolina, Vereinigte Staaten, 27215
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Greensboro, North Carolina, Vereinigte Staaten, 27408
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Morganton, North Carolina, Vereinigte Staaten, 28655
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tabor City, North Carolina, Vereinigte Staaten, 28463
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Pennsylvania
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Johnstown, Pennsylvania, Vereinigte Staaten, 15905
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Levittown, Pennsylvania, Vereinigte Staaten, 19056
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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South Carolina
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Charleston, South Carolina, Vereinigte Staaten, 29412
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tennessee
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Kingsport, Tennessee, Vereinigte Staaten, 37660
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Texas
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Dallas, Texas, Vereinigte Staaten, 75235
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Fort Worth, Texas, Vereinigte Staaten, 76104
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Georgetown, Texas, Vereinigte Staaten, 78626
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Houston, Texas, Vereinigte Staaten, 77074
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Plano, Texas, Vereinigte Staaten, 75023
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Virginia
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Alexandria, Virginia, Vereinigte Staaten, 22304
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Richmond, Virginia, Vereinigte Staaten, 23219
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Cardiff, Vereinigtes Königreich, CF5 4AD
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Chesterfield, Vereinigtes Königreich, S40 4TF
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Avon
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Bath, Avon, Vereinigtes Königreich, BA2 3HT
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Cornwall
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Torpoint, Cornwall, Vereinigtes Königreich, PL11 2JW
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Greater Manchester
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Manchester, Greater Manchester, Vereinigtes Königreich, M20 2RN
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lancashire
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Bolton, Lancashire, Vereinigtes Königreich, BL3 6TL
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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South Yorkshire
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Doncaster, South Yorkshire, Vereinigtes Königreich, DN9 1EP
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Warwickshire
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Atherstone, Warwickshire, Vereinigtes Königreich, CV9 1EU
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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West Glamorgan
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Swansea, West Glamorgan, Vereinigtes Königreich, SA2 8QA
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wiltshire
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Bradford On Avon, Wiltshire, Vereinigtes Königreich, BA15 1DQ
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre und älter (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Probenahmeverfahren
Nicht-Wahrscheinlichkeitsprobe
Studienpopulation
Patienten mit Typ-2-Diabetes, die Primärversorgungs- und Diabetes-Spezialkliniken besuchen.
Beschreibung
Einschlusskriterien:
- Wurde mit Typ-2-Diabetes diagnostiziert
- sich im Rahmen der normalen Pflege vorgestellt haben
- Sie haben ihre anfängliche Insulintherapie für ≥ 3 Monate erhalten (mit oder ohne Kombination von zugelassenen Nicht-Insulin-Antidiabetika)
- nicht gleichzeitig an einer Studie teilnehmen, die ein Prüfpräparat oder -verfahren bei Eintritt in die Studie umfasst
- vollständig aufgeklärt wurden und der Nutzung ihrer Daten schriftlich zugestimmt haben
- Die Hauptsprache des Landes ausreichend verstehen, um die Fragebögen ausfüllen zu können
- Keine basale Bolustherapie begonnen haben (drei Insulininjektionen zu den Mahlzeiten)
Ausschlusskriterien:
- Keiner
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Beobachtungsmodelle: Sonstiges
- Zeitperspektiven: Interessent
Kohorten und Interventionen
Gruppe / Kohorte |
---|
MOSAIC-Teilnehmer
Teilnehmer der Multinational Observational Study Assessing Insulin use (MOSAIc), die während der Studie über vollständige Behandlungsdaten verfügten.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Anzahl der Teilnehmer mit insulinbedingter Behandlungsänderung gegenüber der anfänglichen Insulintherapie
Zeitfenster: Baseline bis 24 Monate
|
Das multivariable logistische Regressionsmodell untersuchte zu Studienbeginn teilnehmer-, arzt- und gesundheitssystembezogene Faktoren im Zusammenhang mit dem Auftreten von Änderungen in der Insulintherapie.
Die Diskriminierungsdomäne des Interpersonal Processes of Care Survey [IPC] reicht von 1-5, wobei höhere Werte mehr Diskriminierung anzeigen, und die Diabetes Distress Scale reicht von 1-6, wobei höhere Werte mehr Stress anzeigen.
|
Baseline bis 24 Monate
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Anzahl hypoglykämischer und schwerer hypoglykämischer Episoden
Zeitfenster: Baseline bis 24 Monate
|
Hypoglykämie und schwere Hypoglykämie-Episoden werden von allen Teilnehmern mit vollständigen Behandlungsdaten von einem Monat vor dem Baseline-Besuch bis zum letzten Besuch (24 Monate) selbst gemeldet.
Die Patienten wurden bei jedem Besuch gebeten, jede Hypoglykämie seit ihrem letzten Besuch selbst zu melden.
Beim Baseline-Besuch wurden die Teilnehmer nach ihren Hypoglykämie-Informationen für den Monat vor dem Baseline-Besuch gefragt.
|
Baseline bis 24 Monate
|
Anzahl der Teilnehmer, die sich während der Studie an die verschriebene Insulintherapie hielten (Studienteilnehmer)
Zeitfenster: Baseline bis 24 Monate
|
Die MOSAIC-Teilnehmer beantworteten die Frage: „Wie oft haben Sie Ihre Insulinspritzen in den letzten 7 Tagen verpasst?“.
Bei jedem Besuch wurden die Teilnehmer als besuchswillig definiert, wenn der Teilnehmer antwortete „Ich habe keine Aufnahmen verpasst“ oder „Ich habe einige meiner Aufnahmen verpasst“.
Sie wurden als nicht an einem Besuch teilnehmend definiert, wenn er/sie eine der folgenden Antworten gab: „Ich habe ungefähr die Hälfte meiner Aufnahmen verpasst“, „Ich habe die meisten meiner Aufnahmen verpasst“ oder „Ich habe alle meine Aufnahmen verpasst“.
Ein Teilnehmer wird als studienadhärent definiert, wenn mindestens: 4 von 5 Visitadhärenten sind.
|
Baseline bis 24 Monate
|
Anzahl der Teilnehmer, die am Ende der Studie ihren personalisierten HbA1c-Zielwert erreicht haben
Zeitfenster: Baseline bis 24 Monate
|
Da die Diabetes-Managementpraktiken in den in MOSAIC vertretenen Ländern unterschiedlich sind, ist ein geeigneterer Maßstab für das Erreichen des Ziels das personalisierte Ziel, das für jeden Patienten zu Beginn der Studie festgelegt wurde.
|
Baseline bis 24 Monate
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Allgemeine Veröffentlichungen
- Matsuba I, Kawata T, Ajima M, Umezawa S, Kaneshiro M, Asakura T, Machimura H, Sawa T, Tanaka K, Takeda H, Imaoka T, Kanamori A. Multinational Observational Study to Understand Insulin Treatment Intensification: Japanese Subgroup Analysis of the MOSAIc Study. Diabetes Ther. 2022 Feb;13(2):265-274. doi: 10.1007/s13300-021-01195-8. Epub 2022 Jan 6.
- Caballero AE, Nordstrom BL, Liao B, Fan L, Zhang N, Fraeman KH, Perez-Nieves M. Individualized HbA1c target selection and achievement in the Multinational Observational Study Assessing Insulin Use (MOSA1c) type 2 diabetes study. J Diabetes Complications. 2021 Nov;35(11):108011. doi: 10.1016/j.jdiacomp.2021.108011. Epub 2021 Jul 30.
- Linetzky B, Curtis B, Frechtel G, Montenegro R Jr, Escalante Pulido M, Stempa O, de Lana JM, Gagliardino JJ. Challenges associated with insulin therapy progression among patients with type 2 diabetes: Latin American MOSAIc study baseline data. Diabetol Metab Syndr. 2016 Jul 22;8:41. doi: 10.1186/s13098-016-0157-1. eCollection 2016.
- Matsuba I, Sawa T, Kawata T, Kanamori A, Jiang D, Machimura H, Takeda H, Han JH, Wang K, Tanaka K, Shen L, Ajima M, Kaneshiro M, Kim SW, Umezawa S, Asakura T, Suzuki S, Kim SC. Cross-National Variation in Glycemic Control and Diabetes-Related Distress Among East Asian Patients Using Insulin: Results from the MOSAIc Study. Diabetes Ther. 2016 Jun;7(2):349-60. doi: 10.1007/s13300-016-0178-7. Epub 2016 Jun 2.
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. Juli 2011
Primärer Abschluss (Tatsächlich)
1. September 2015
Studienabschluss (Tatsächlich)
1. September 2015
Studienanmeldedaten
Zuerst eingereicht
21. Juli 2011
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
21. Juli 2011
Zuerst gepostet (Schätzen)
25. Juli 2011
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
9. März 2020
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
25. Februar 2020
Zuletzt verifiziert
1. Februar 2020
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 14056
- F3Z-MC-B010 (Andere Kennung: Eli Lilly and Company)
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Nein
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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