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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

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

      • 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
        • 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.
      • Mumbai, Indien, 400053
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      • Mysore, Indien, 570023
        • 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.
      • 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
        • 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.
      • Beer Yaakov, Israel, 70300
        • 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.
      • Dimona, Israel, 68000
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      • Givataim, Israel, 53488
        • 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.
      • Netanya, Israel, 42470
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      • Petach Tikwa, Israel, 49582
        • 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.
      • 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
      • Edmonton, Alberta, Kanada, T5A 4L8
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      • Spruce Grove, Alberta, Kanada, T7X 2V2
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    • Manitoba
      • Winnipeg, Manitoba, Kanada, R3C 0N2
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    • Newfoundland and Labrador
      • St. John'S, Newfoundland and Labrador, Kanada, A1A3R5
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    • Ontario
      • 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
      • 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
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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
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      • Rio Piedras, Puerto Rico, 00921
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      • San Juan, Puerto Rico, 00920
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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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • Makkah, Saudi-Arabien, 21955
        • 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.
      • Riyadh, Saudi-Arabien, 245
        • 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.
      • 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.
      • 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.
      • Gerena, Spanien
        • 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.
      • 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.
      • Madrid, Spanien, 28034
        • 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.
      • Sevilla, Spanien, 41009
        • 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.
      • Vic, Spanien, 08500
        • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
    • Arkansas
      • 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.
    • Florida
      • 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.
      • 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.
    • Georgia
      • 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.
    • Illinois
      • 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.
    • Nebraska
      • 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.
    • Nevada
      • 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.
    • North Carolina
      • 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.
      • 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.
      • 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.
      • 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.
    • Pennsylvania
      • 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.
      • 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.
    • South Carolina
      • 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.
    • Tennessee
      • 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.
    • Texas
      • 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.
      • 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.
      • 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.
      • 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.
      • 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.
    • Virginia
      • 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.
      • 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.
      • 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.
      • 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.
    • Avon
      • 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.
    • Cornwall
      • 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.
    • Greater Manchester
      • 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.
    • Lancashire
      • 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.
    • South Yorkshire
      • 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.
    • Warwickshire
      • 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.
    • West Glamorgan
      • 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.
    • Wiltshire
      • 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.

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.

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.

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

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 .

Klinische Studien zur Diabetes mellitus, Typ 2

3
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