ID
29449
Beschrijving
Effect of 4 Weeks Treatment With Acipimox in Patients With Chronic Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00549614
Link
https://clinicaltrials.gov/show/NCT00549614
Trefwoorden
Versies (1)
- 26-03-18 26-03-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
26 maart 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Heart Failure NCT00549614
Eligibility Heart Failure NCT00549614
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Pregnancy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
Beschrijving
Kidney Failure Severe
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0035078
- UMLS CUI [1,2]
- C0205082
Beschrijving
Bradyarrhythmia | Tachyarrhythmia
Datatype
boolean
Alias
- UMLS CUI [1]
- C0079035
- UMLS CUI [2]
- C0080203
Beschrijving
Valvular Stenosis Severe
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1883524
- UMLS CUI [1,2]
- C0205082
Beschrijving
Myocardial Infarction
Datatype
boolean
Alias
- UMLS CUI [1]
- C0027051
Beschrijving
Insulin regime Diabetes Mellitus
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0557978
- UMLS CUI [1,2]
- C0011849
Beschrijving
Peptic Ulcer
Datatype
boolean
Alias
- UMLS CUI [1]
- C0030920
Beschrijving
Pregnancy | Breast Feeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Beschrijving
Hypersensitivity Investigational New Drugs
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0013230
Similar models
Eligibility Heart Failure NCT00549614
- StudyEvent: Eligibility
C0205082 (UMLS CUI [1,2])
C0080203 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C0011849 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0013230 (UMLS CUI [1,2])