Eligibility Type 2 Diabetes NCT01757587

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients treated for at least 3 months with metformin (at the maximum tolerated dose (for at least 1 month) + / - sulfamide and basal insulin
Beskrivning

Metformin Maximum Tolerated Dose | Sulfonamides | Basal insulin

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0025598
UMLS CUI [1,2]
C0752079
UMLS CUI [2]
C0038760
UMLS CUI [3]
C0650607
patient with an hba1c between 7 and 9% at the inclusion visit
Beskrivning

Hemoglobin A1c measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0474680
patients able to use a continuous glucose monitoring system,
Beskrivning

Use of Glucose measurement by monitoring device

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C0202048
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients already receiving a specific treatment of postprandial (glp1, ..)
Beskrivning

Therapeutic procedure Postprandial | Glucagon-Like Peptide 1

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0376674
UMLS CUI [2]
C0061355
patients with type 1 diabetes, or secondary diabetes
Beskrivning

Diabetes Mellitus, Insulin-Dependent | Secondary diabetes mellitus

Datatyp

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0271640
patients with eating disorders
Beskrivning

Eating Disorders

Datatyp

boolean

Alias
UMLS CUI [1]
C0013473
patients with major complications of diabetes
Beskrivning

Complications of Diabetes Mellitus Major

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0342257
UMLS CUI [1,2]
C0205164
patients participating in another clinical trial
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
pregnant
Beskrivning

Pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961

Similar models

Eligibility Type 2 Diabetes NCT01757587

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
Study Subject Participation Status
Item
patients participating in another clinical trial
boolean
C2348568 (UMLS CUI [1])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])