ID
36141
Description
Prevention of Severe Postpartum Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02450773
Link
https://clinicaltrials.gov/show/NCT02450773
Keywords
Versions (1)
- 4/17/19 4/17/19 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
April 17, 2019
DOI
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License
Creative Commons BY 4.0
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Eligibility Hypertension NCT02450773
Eligibility Hypertension NCT02450773
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Hypertension chronic
Data type
boolean
Alias
- UMLS CUI [1]
- C0745114
Description
Furosemide allergy
Data type
boolean
Alias
- UMLS CUI [1]
- C0571903
Description
Hypokalemia Pre-existing | Serum potassium measurement
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020621
- UMLS CUI [1,2]
- C2347662
- UMLS CUI [2]
- C0302353
Description
Chronic Kidney Disease
Data type
boolean
Alias
- UMLS CUI [1]
- C1561643
Description
Creatinine measurement, serum
Data type
boolean
Alias
- UMLS CUI [1]
- C0201976
Description
Informed Consent Unable
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1299582
Description
Use of Diuretics Pre-existing
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1524063
- UMLS CUI [1,2]
- C0012798
- UMLS CUI [1,3]
- C2347662
Description
Oliguria
Data type
boolean
Alias
- UMLS CUI [1]
- C0028961
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Eligibility Hypertension NCT02450773
- StudyEvent: Eligibility
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C1135241 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0852036 (UMLS CUI [1,2])
C0032914 (UMLS CUI [1,2])
C0341950 (UMLS CUI [1,2])
C0332282 (UMLS CUI [1,2])
C0011209 (UMLS CUI [1,3])
C2347662 (UMLS CUI [1,2])
C0302353 (UMLS CUI [2])
C1299582 (UMLS CUI [1,2])
C0012798 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])