ID
34669
Description
An 8-week Study to Evaluate the Dose Response of AHU377 in Combination With Valsartan 320 mg in Patients With Mild-to-moderate Systolic Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01281306
Lien
https://clinicaltrials.gov/show/NCT01281306
Mots-clés
Versions (1)
- 22/01/2019 22/01/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
22 janvier 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Systolic Hypertension NCT01281306
Eligibility Systolic Hypertension NCT01281306
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Hypertension, severe
Type de données
boolean
Alias
- UMLS CUI [1]
- C4013784
Description
Angioedema Drug-induced | Angioedema
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0002994
- UMLS CUI [1,2]
- C0458082
- UMLS CUI [2]
- C0002994
Description
Pregnancy | Breast Feeding
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Childbearing Potential | Exception Use of Contraceptive methods
Type de données
boolean
Alias
- UMLS CUI [1]
- C3831118
- UMLS CUI [2,1]
- C1705847
- UMLS CUI [2,2]
- C1524063
- UMLS CUI [2,3]
- C0700589
Description
Secondary hypertension
Type de données
boolean
Alias
- UMLS CUI [1]
- C0155616
Description
Eligibility Criteria Study Protocol
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1516637
- UMLS CUI [1,2]
- C2348563
Similar models
Eligibility Systolic Hypertension NCT01281306
- StudyEvent: Eligibility
C1845210 (UMLS CUI [2])
C0221155 (UMLS CUI [3,1])
C0205081 (UMLS CUI [3,2])
C0332155 (UMLS CUI [4])
C0585941 (UMLS CUI [5])
C0525058 (UMLS CUI [2])
C3489773 (UMLS CUI [3,1])
C0205170 (UMLS CUI [3,2])
C0458082 (UMLS CUI [1,2])
C0002994 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C1705847 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
C0700589 (UMLS CUI [2,3])
C2348563 (UMLS CUI [1,2])