ID
36141
Beschrijving
Prevention of Severe Postpartum Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02450773
Link
https://clinicaltrials.gov/show/NCT02450773
Trefwoorden
Versies (1)
- 17-04-19 17-04-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
17 april 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT02450773
Eligibility Hypertension NCT02450773
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Hypertension chronic
Datatype
boolean
Alias
- UMLS CUI [1]
- C0745114
Beschrijving
Furosemide allergy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0571903
Beschrijving
Hypokalemia Pre-existing | Serum potassium measurement
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020621
- UMLS CUI [1,2]
- C2347662
- UMLS CUI [2]
- C0302353
Beschrijving
Chronic Kidney Disease
Datatype
boolean
Alias
- UMLS CUI [1]
- C1561643
Beschrijving
Creatinine measurement, serum
Datatype
boolean
Alias
- UMLS CUI [1]
- C0201976
Beschrijving
Informed Consent Unable
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1299582
Beschrijving
Use of Diuretics Pre-existing
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1524063
- UMLS CUI [1,2]
- C0012798
- UMLS CUI [1,3]
- C2347662
Beschrijving
Oliguria
Datatype
boolean
Alias
- UMLS CUI [1]
- C0028961
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Eligibility Hypertension NCT02450773
- StudyEvent: Eligibility
C1135241 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0007876 (UMLS CUI [2,1])
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])