ID
29465
Description
OVATIO CRT and SITUS OTW LV Lead Post Approval Study; ODM derived from: https://clinicaltrials.gov/show/NCT00795873
Link
https://clinicaltrials.gov/show/NCT00795873
Keywords
Versions (2)
- 3/28/18 3/28/18 -
- 9/20/21 9/20/21 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
March 28, 2018
DOI
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License
Creative Commons BY 4.0
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Eligibility Heart Failure NCT00795873
Eligibility Heart Failure NCT00795873
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Ventricular Tachycardia Cause Transient | Ventricular Tachycardia Cause Reversible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0042514
- UMLS CUI [1,2]
- C0015127
- UMLS CUI [1,3]
- C0205374
- UMLS CUI [2,1]
- C0042514
- UMLS CUI [2,2]
- C0015127
- UMLS CUI [2,3]
- C0205343
Description
Incessant ventricular tachycardia
Data type
boolean
Alias
- UMLS CUI [1]
- C2363809
Description
Implant Lead Coronary sinus
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021102
- UMLS CUI [1,2]
- C1704733
- UMLS CUI [1,3]
- C0456944
Description
Myocardial Revascularization | Angioplasty
Data type
boolean
Alias
- UMLS CUI [1]
- C0027056
- UMLS CUI [2]
- C0162577
Description
Heart failure Due to Valvular disease | Valvular disease Correction Possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0678226
- UMLS CUI [1,3]
- C3258293
- UMLS CUI [2,1]
- C3258293
- UMLS CUI [2,2]
- C1947976
- UMLS CUI [2,3]
- C0332149
Description
Atrial tachycardia chronic refractory
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0546959
- UMLS CUI [1,2]
- C0205191
- UMLS CUI [1,3]
- C0205269
Description
Study Subject Participation Status Interferes with Research results
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C0521102
- UMLS CUI [1,3]
- C0683954
Description
Life Expectancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0023671
Description
Study Protocol Comprehension Unable | Patient cooperation Refused
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348563
- UMLS CUI [1,2]
- C0162340
- UMLS CUI [1,3]
- C1299582
- UMLS CUI [2,1]
- C1321605
- UMLS CUI [2,2]
- C1705116
Description
Informed Consent Unable | Informed Consent Refused
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1299582
- UMLS CUI [2,1]
- C0021430
- UMLS CUI [2,2]
- C1705116
Description
Patient unavailable Follow-up | Patient unavailable Implantation procedure
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1301818
- UMLS CUI [1,2]
- C3274571
- UMLS CUI [2,1]
- C1301818
- UMLS CUI [2,2]
- C0021107
Description
Hypersensitivity Dexamethasone sodium phosphate Dose
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0113286
- UMLS CUI [1,3]
- C0178602
Description
Age
Data type
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
Pregnancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
Similar models
Eligibility Heart Failure NCT00795873
- StudyEvent: Eligibility
C0205360 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,2])
C0205374 (UMLS CUI [1,3])
C0042514 (UMLS CUI [2,1])
C0015127 (UMLS CUI [2,2])
C0205343 (UMLS CUI [2,3])
C1704733 (UMLS CUI [1,2])
C0456944 (UMLS CUI [1,3])
C0162577 (UMLS CUI [2])
C0678226 (UMLS CUI [1,2])
C3258293 (UMLS CUI [1,3])
C3258293 (UMLS CUI [2,1])
C1947976 (UMLS CUI [2,2])
C0332149 (UMLS CUI [2,3])
C0205191 (UMLS CUI [1,2])
C0205269 (UMLS CUI [1,3])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1321605 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C3274571 (UMLS CUI [1,2])
C1301818 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
C0113286 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])