ID

34594

Beschrijving

Study of ITCA 650 (Exenatide in DUROS) in Subjects With Type 2 Diabetes Mellitus; ODM derived from: https://clinicaltrials.gov/show/NCT00943917

Link

https://clinicaltrials.gov/show/NCT00943917

Trefwoorden

  1. 19-01-19 19-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes NCT00943917

Eligibility Type 2 Diabetes NCT00943917

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
males or females age 18-70 years
Beschrijving

ID.1

Datatype

boolean

type 2 diabetes mellitus for ≥ 6 months prior to screening visit 1
Beschrijving

ID.2

Datatype

boolean

on a stable (> 3 months prior to screening visit 1) treatment regimen of metformin monotherapy;
Beschrijving

ID.3

Datatype

boolean

fasting plasma glucose < 240 mg/dl at screening visit 1
Beschrijving

ID.4

Datatype

boolean

hba1c ≥ 7% and ≤ 10% at screening visit 1
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior treatment with exenatide
Beschrijving

ID.6

Datatype

boolean

treatment with any of the following antidiabetic agents within 3 months prior to screening visit 1: tzds, sulfonylureas, dpp iv inhibitors, acarbose, or insulin (injected or inhaled)
Beschrijving

ID.7

Datatype

boolean

history of type 1 diabetes and/or history of diabetic ketoacidosis
Beschrijving

ID.8

Datatype

boolean

body mass index ≥ 40 kg/m2;
Beschrijving

ID.9

Datatype

boolean

history of organ transplantation
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Type 2 Diabetes NCT00943917

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
males or females age 18-70 years
boolean
ID.2
Item
type 2 diabetes mellitus for ≥ 6 months prior to screening visit 1
boolean
ID.3
Item
on a stable (> 3 months prior to screening visit 1) treatment regimen of metformin monotherapy;
boolean
ID.4
Item
fasting plasma glucose < 240 mg/dl at screening visit 1
boolean
ID.5
Item
hba1c ≥ 7% and ≤ 10% at screening visit 1
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
prior treatment with exenatide
boolean
ID.7
Item
treatment with any of the following antidiabetic agents within 3 months prior to screening visit 1: tzds, sulfonylureas, dpp iv inhibitors, acarbose, or insulin (injected or inhaled)
boolean
ID.8
Item
history of type 1 diabetes and/or history of diabetic ketoacidosis
boolean
ID.9
Item
body mass index ≥ 40 kg/m2;
boolean
ID.10
Item
history of organ transplantation
boolean

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