ID

27657

Description

The Indian POLYCAP Study (TIPS); ODM derived from: https://clinicaltrials.gov/show/NCT00443794

Link

https://clinicaltrials.gov/show/NCT00443794

Keywords

Versions (1)
  1. 11/25/17 11/25/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 25, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Cardiovascular Diseases NCT00443794

English

Eligibility Cardiovascular Diseases NCT00443794

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age between 45 and 80 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
at least any one of the following cvd risk factors:
Description

Cardiovascular Diseases Risk factors Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0035648
UMLS CUI [1,3]
C1265611
stable type 2 diabetes mellitus or
Description

Non-Insulin-Dependent Diabetes Mellitus Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0011860
UMLS CUI [1,2]
C0205360
hypertension or
Description

Hypertensive disease

Data type

boolean

Alias
UMLS CUI [1]
C0020538
current smoker or
Description

Tobacco use

Data type

boolean

Alias
UMLS CUI [1]
C0543414
a waist to hip ratio > 0.85 for women and >0.9 for men or
Description

Waist-Hip Ratio | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0205682
UMLS CUI [2]
C0079399
elevated lipids.
Description

Raised serum lipid levels

Data type

boolean

Alias
UMLS CUI [1]
C0856968
informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
on any of the study medications,
Description

Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C0013230
uncontrolled blood pressure,
Description

Blood Pressure Uncontrolled

Data type

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C0205318
symptomatic hypotension,
Description

Hypotension symptomatic

Data type

boolean

Alias
UMLS CUI [1]
C0863113
any clear indication or a contraindication to the use of any of the study medications,
Description

Indication Investigational New Drugs | Medical contraindication Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0013230
history of coronary/cerebrovascular events,
Description

Coronary disorder | Cerebrovascular accident

Data type

boolean

Alias
UMLS CUI [1]
C0010068
UMLS CUI [2]
C0038454
pregnancy or lactating or women of child-bearing potential with inadequate contraception and / or an inability to attend follow up visits.
Description

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Inadequate | Childbearing Potential Follow-up visit Unable

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0205412
UMLS CUI [4,1]
C3831118
UMLS CUI [4,2]
C0589121
UMLS CUI [4,3]
C1299582
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Similar models

Eligibility Cardiovascular Diseases NCT00443794

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
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])
Non-Insulin-Dependent Diabetes Mellitus Stable
Item
stable type 2 diabetes mellitus or
boolean
C0011860 (UMLS CUI [1,1])
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])
Raised serum lipid levels
Item
elevated lipids.
boolean
C0856968 (UMLS CUI [1])
Informed Consent
Item
informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
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])
Coronary disorder | Cerebrovascular accident
Item
history of coronary/cerebrovascular events,
boolean
C0010068 (UMLS CUI [1])
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])
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