ID
23460
Description
Efficacy and Safety Study on Agilis NxT Introducer in AF Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00469638
Link
https://clinicaltrials.gov/show/NCT00469638
Keywords
Versions (1)
- 7/5/17 7/5/17 -
Uploaded on
July 5, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00469638
Eligibility Atrial Fibrillation NCT00469638
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Permanent atrial fibrillation
Data type
boolean
Alias
- UMLS CUI [1]
- C2586056
Description
Ablation for atrial fibrillation Left Pre-existing
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2702800
- UMLS CUI [1,2]
- C0225860
- UMLS CUI [1,3]
- C2347662
Description
Atrial Fibrillation Due to Cause Reversible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0004238
- UMLS CUI [1,2]
- C0678226
- UMLS CUI [1,3]
- C0015127
- UMLS CUI [1,4]
- C0205343
Description
Intracardiac thrombus | Thrombus
Data type
boolean
Alias
- UMLS CUI [1]
- C0876998
- UMLS CUI [2]
- C0087086
Description
Pregnancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
Description
Childbearing Potential Pregnancy test negative Lacking
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3831118
- UMLS CUI [1,2]
- C0427780
- UMLS CUI [1,3]
- C0332268
Description
Medical contraindication Anticoagulation
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0003281
Similar models
Eligibility Atrial Fibrillation NCT00469638
- StudyEvent: Eligibility
C2585653 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C1265611 (UMLS CUI [1,2])
C0332325 (UMLS CUI [1,3])
C1301886 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
C0430462 (UMLS CUI [2,1])
C0442146 (UMLS CUI [2,2])
C0444868 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,3])
C0470187 (UMLS CUI [1,4])
C0225860 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])
C0678226 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0205343 (UMLS CUI [1,4])
C0087086 (UMLS CUI [2])
C0427780 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C0003281 (UMLS CUI [1,2])