ID

34272

Beschrijving

Evaluate Adherence to Treatment With Glucophage Sachets Versus Tablets in Diabetes Type 2 Patients Previously Treated With Metformin Tablets; ODM derived from: https://clinicaltrials.gov/show/NCT01510522

Link

https://clinicaltrials.gov/show/NCT01510522

Trefwoorden

  1. 16-01-19 16-01-19 -
  2. 14-05-19 14-05-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Diabetes Mellitus Type 2 NCT01510522

Eligibility Diabetes Mellitus Type 2 NCT01510522

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diabetes mellitus type 2 diagnosed (baseline glycemia > 7,0 mmol/l (126 mg/dl) or overload glycemia > 11,0 mmol/l (198 mg/dl)
Beschrijving

ID.1

Datatype

boolean

on treatment with metformin tablets
Beschrijving

ID.2

Datatype

boolean

patients with at least 2 treated co-morbidities
Beschrijving

ID.3

Datatype

boolean

established dose of metformin > 1.700 mg/day
Beschrijving

ID.4

Datatype

boolean

age > 18 years old
Beschrijving

ID.5

Datatype

boolean

given informed consent
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients not able to take medication orally
Beschrijving

ID.7

Datatype

boolean

according to summary of product characteristics (smpc)
Beschrijving

ID.8

Datatype

boolean

participating in another clinical trial 30 days prior to randomization
Beschrijving

ID.9

Datatype

boolean

any other illness or medical or psychiatric condition, severe and uncontrolled that could interfere in the patient's participation or in the assessment of the study results
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Diabetes Mellitus Type 2 NCT01510522

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diabetes mellitus type 2 diagnosed (baseline glycemia > 7,0 mmol/l (126 mg/dl) or overload glycemia > 11,0 mmol/l (198 mg/dl)
boolean
ID.2
Item
on treatment with metformin tablets
boolean
ID.3
Item
patients with at least 2 treated co-morbidities
boolean
ID.4
Item
established dose of metformin > 1.700 mg/day
boolean
ID.5
Item
age > 18 years old
boolean
ID.6
Item
given informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
patients not able to take medication orally
boolean
ID.8
Item
according to summary of product characteristics (smpc)
boolean
ID.9
Item
participating in another clinical trial 30 days prior to randomization
boolean
ID.10
Item
any other illness or medical or psychiatric condition, severe and uncontrolled that could interfere in the patient's participation or in the assessment of the study results
boolean

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