Informatie:
Fout:
ID
27657
Beschrijving
The Indian POLYCAP Study (TIPS); ODM derived from: https://clinicaltrials.gov/show/NCT00443794
Link
https://clinicaltrials.gov/show/NCT00443794
Trefwoorden
Versies (1)
- 25-11-17 25-11-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
25 november 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Cardiovascular Diseases NCT00443794
Eligibility Cardiovascular Diseases NCT00443794
- StudyEvent: Eligibility
Similar models
Eligibility Cardiovascular Diseases NCT00443794
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
age between 45 and 80 years
boolean
C0001779 (UMLS CUI [1])
Cardiovascular Diseases Risk factors Quantity
Item
at least any one of the following cvd risk factors:
boolean
C0007222 (UMLS CUI [1,1])
C0035648 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0035648 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Non-Insulin-Dependent Diabetes Mellitus Stable
Item
stable type 2 diabetes mellitus or
boolean
C0011860 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,2])
Hypertensive disease
Item
hypertension or
boolean
C0020538 (UMLS CUI [1])
Tobacco use
Item
current smoker or
boolean
C0543414 (UMLS CUI [1])
Waist-Hip Ratio | Gender
Item
a waist to hip ratio > 0.85 for women and >0.9 for men or
boolean
C0205682 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0079399 (UMLS CUI [2])
Raised serum lipid levels
Item
elevated lipids.
boolean
C0856968 (UMLS CUI [1])
Informed Consent
Item
informed consent.
boolean
C0021430 (UMLS CUI [1])
Investigational New Drugs
Item
on any of the study medications,
boolean
C0013230 (UMLS CUI [1])
Blood Pressure Uncontrolled
Item
uncontrolled blood pressure,
boolean
C0005823 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,2])
Hypotension symptomatic
Item
symptomatic hypotension,
boolean
C0863113 (UMLS CUI [1])
Indication Investigational New Drugs | Medical contraindication Investigational New Drugs
Item
any clear indication or a contraindication to the use of any of the study medications,
boolean
C3146298 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Coronary disorder | Cerebrovascular accident
Item
history of coronary/cerebrovascular events,
boolean
C0010068 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0038454 (UMLS CUI [2])
Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Inadequate | Childbearing Potential Follow-up visit Unable
Item
pregnancy or lactating or women of child-bearing potential with inadequate contraception and / or an inability to attend follow up visits.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0205412 (UMLS CUI [3,3])
C3831118 (UMLS CUI [4,1])
C0589121 (UMLS CUI [4,2])
C1299582 (UMLS CUI [4,3])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0205412 (UMLS CUI [3,3])
C3831118 (UMLS CUI [4,1])
C0589121 (UMLS CUI [4,2])
C1299582 (UMLS CUI [4,3])