ID
41394
Beschrijving
Diuretics for Postpartum High Blood Pressure in Preeclampsia; ODM derived from: https://clinicaltrials.gov/show/NCT02163655
Link
https://clinicaltrials.gov/show/NCT02163655
Trefwoorden
Versies (3)
- 17-01-19 17-01-19 -
- 28-09-20 28-09-20 -
- 28-09-20 28-09-20 -
Houder van rechten
see on clinicaltrials.gov
Geüploaded op
28 september 2020
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Postpartum High Blood Pressure in Preeclampsia NCT02163655
Eligibility Postpartum High Blood Pressure in Preeclampsia NCT02163655
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Chronic hypertension
Datatype
boolean
Alias
- UMLS CUI [1]
- C0745114
Beschrijving
Blood pressure
Datatype
boolean
Alias
- UMLS CUI [1]
- C0428883
- UMLS CUI [2]
- C0871470
Beschrijving
Use of diuretics
Datatype
boolean
Alias
- UMLS CUI [1]
- C0012798
Beschrijving
Renal impairment
Datatype
boolean
Alias
- UMLS CUI [1]
- C1565489
Beschrijving
Diabetes, sickle cell disease or rheumatologie disease
Datatype
boolean
Alias
- UMLS CUI [1]
- C0011849
- UMLS CUI [2]
- C0002895
- UMLS CUI [3]
- C0035435
Beschrijving
Hemodynamic instability
Datatype
boolean
Alias
- UMLS CUI [1]
- C0948268
Beschrijving
Potassium
Datatype
boolean
Alias
- UMLS CUI [1]
- C0202194
Beschrijving
Contraindications for furosemide
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0016860
- UMLS CUI [1,2]
- C0522473
Similar models
Eligibility Postpartum High Blood Pressure in Preeclampsia NCT02163655
- StudyEvent: Eligibility
C0086839 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0871470 (UMLS CUI [2])
C0002895 (UMLS CUI [2])
C0035435 (UMLS CUI [3])
C0522473 (UMLS CUI [1,2])