Information:
Fel:
ID
34756
Beskrivning
Galvus (Vildagliptin) vs Placebo in Combination With Metformin and Insulin; ODM derived from: https://clinicaltrials.gov/show/NCT01757587
Länk
https://clinicaltrials.gov/show/NCT01757587
Nyckelord
Versioner (1)
- 2019-01-27 2019-01-27 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
27 januari 2019
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Type 2 Diabetes NCT01757587
Eligibility Type 2 Diabetes NCT01757587
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes NCT01757587
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Metformin Maximum Tolerated Dose | Sulfonamides | Basal insulin
Item
patients treated for at least 3 months with metformin (at the maximum tolerated dose (for at least 1 month) + / - sulfamide and basal insulin
boolean
C0025598 (UMLS CUI [1,1])
C0752079 (UMLS CUI [1,2])
C0038760 (UMLS CUI [2])
C0650607 (UMLS CUI [3])
C0752079 (UMLS CUI [1,2])
C0038760 (UMLS CUI [2])
C0650607 (UMLS CUI [3])
Hemoglobin A1c measurement
Item
patient with an hba1c between 7 and 9% at the inclusion visit
boolean
C0474680 (UMLS CUI [1])
Use of Glucose measurement by monitoring device
Item
patients able to use a continuous glucose monitoring system,
boolean
C1524063 (UMLS CUI [1,1])
C0202048 (UMLS CUI [1,2])
C0202048 (UMLS CUI [1,2])
Therapeutic procedure Postprandial | Glucagon-Like Peptide 1
Item
patients already receiving a specific treatment of postprandial (glp1, ..)
boolean
C0087111 (UMLS CUI [1,1])
C0376674 (UMLS CUI [1,2])
C0061355 (UMLS CUI [2])
C0376674 (UMLS CUI [1,2])
C0061355 (UMLS CUI [2])
Diabetes Mellitus, Insulin-Dependent | Secondary diabetes mellitus
Item
patients with type 1 diabetes, or secondary diabetes
boolean
C0011854 (UMLS CUI [1])
C0271640 (UMLS CUI [2])
C0271640 (UMLS CUI [2])
Eating Disorders
Item
patients with eating disorders
boolean
C0013473 (UMLS CUI [1])
Complications of Diabetes Mellitus Major
Item
patients with major complications of diabetes
boolean
C0342257 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,2])
Study Subject Participation Status
Item
patients participating in another clinical trial
boolean
C2348568 (UMLS CUI [1])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])