ID
44433
Description
QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization; ODM derived from: https://clinicaltrials.gov/show/NCT00918294
Link
https://clinicaltrials.gov/show/NCT00918294
Keywords
Versions (2)
- 3/29/18 3/29/18 -
- 9/20/21 9/20/21 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
September 20, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility Heart Failure NCT00918294
Eligibility Heart Failure NCT00918294
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Atrium Activity Intrinsic Limited
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0018792
- UMLS CUI [1,2]
- C0205177
- UMLS CUI [1,3]
- C0205102
- UMLS CUI [1,4]
- C0439801
Description
Persistent atrial fibrillation | Permanent atrial fibrillation
Data type
boolean
Alias
- UMLS CUI [1]
- C2585653
- UMLS CUI [2]
- C2586056
Description
Second degree atrioventricular block | Complete atrioventricular block
Data type
boolean
Alias
- UMLS CUI [1]
- C0264906
- UMLS CUI [2]
- C0151517
Description
Echocardiogram (image) Unable
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2243117
- UMLS CUI [1,2]
- C1299582
Description
Life Expectancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0023671
Description
Age
Data type
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
Pregnancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
Description
Inotropic agent Intravenous
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0304509
- UMLS CUI [1,2]
- C1522726
Similar models
Eligibility Heart Failure NCT00918294
- StudyEvent: Eligibility
C1737639 (UMLS CUI [1,2])
C0021107 (UMLS CUI [2,1])
C1737639 (UMLS CUI [2,2])
C0021107 (UMLS CUI [3,1])
C0181586 (UMLS CUI [3,2])
C3888058 (UMLS CUI [3,3])
C1524057 (UMLS CUI [3,4])
C0205177 (UMLS CUI [1,2])
C0205102 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,4])
C2586056 (UMLS CUI [2])
C0151517 (UMLS CUI [2])
C1299582 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,2])