ID
12771
Description
Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Intervention; ODM derived from: https://clinicaltrials.gov/show/NCT01230606
Link
https://clinicaltrials.gov/show/NCT01230606
Keywords
Versions (1)
- 12/21/15 12/21/15 -
Uploaded on
December 21, 2015
DOI
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License
Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT01230606
Eligibility Cardiovascular Disease NCT01230606
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
life expectancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0023671
Description
acute coronary syndrome
Data type
boolean
Alias
- UMLS CUI [1]
- C0948089
Description
access femoral
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0444454
- UMLS CUI [1,2]
- C0015811
Description
anticoagulants
Data type
boolean
Alias
- UMLS CUI [1]
- C0003280
Description
Percutaneous Coronary Intervention; angiogram
Data type
boolean
Alias
- UMLS CUI [1]
- C1532338
- UMLS CUI [2]
- C0002978
Description
Percutaneous Coronary Intervention; Coronary artery
Data type
boolean
Alias
- UMLS CUI [1]
- C1532338
- UMLS CUI [2]
- C0205042
Description
thrombus; angiogram
Data type
boolean
Alias
- UMLS CUI [1]
- C0087086
- UMLS CUI [2]
- C0002978
Description
stent; Percutaneous Coronary Intervention
Data type
boolean
Alias
- UMLS CUI [1]
- C0038257
- UMLS CUI [2]
- C1532338
Description
International Normalized Ratio; Platelet Count measurement; Platelet hematocrit measurement
Data type
boolean
Alias
- UMLS CUI [1]
- C0525032
- UMLS CUI [2]
- C0032181
- UMLS CUI [3]
- C0474566
Description
occlusion; Percutaneous Coronary Intervention
Data type
boolean
Alias
- UMLS CUI [1]
- C1947917
- UMLS CUI [2]
- C1532338
Description
ejection fraction
Data type
boolean
Alias
- UMLS CUI [1]
- C0232174
Description
hypersensitivity Percutaneous Coronary Intervention medication
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C1532338
- UMLS CUI [1,3]
- C0013227
Description
residence patient
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0237096
- UMLS CUI [1,2]
- C0030705
Description
informed consent
Data type
boolean
Alias
- UMLS CUI [1]
- C0021430
Description
vascular complication
Data type
boolean
Alias
- UMLS CUI [1]
- C1112391
Description
pregnant
Data type
boolean
Alias
- UMLS CUI [1]
- C0549206
Description
infection
Data type
boolean
Alias
- UMLS CUI [1]
- C0009450
Description
chronic renal insufficiency
Data type
boolean
Alias
- UMLS CUI [1]
- C0022661
Similar models
Eligibility Cardiovascular Disease NCT01230606
- StudyEvent: Eligibility
C0015811 (UMLS CUI [1,2])
C0002978 (UMLS CUI [2])
C0205042 (UMLS CUI [2])
C0002978 (UMLS CUI [2])
C1532338 (UMLS CUI [2])
C0032181 (UMLS CUI [2])
C0474566 (UMLS CUI [3])
C1532338 (UMLS CUI [2])
C1532338 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0030705 (UMLS CUI [1,2])