ID
16797
Description
Assessment of Efficacy and Safety of Olmesartan Medoxomil in Children and Adolescent Patients With High Blood Pressure; ODM derived from: https://clinicaltrials.gov/show/NCT00151775
Lien
https://clinicaltrials.gov/show/NCT00151775
Mots-clés
Versions (1)
- 07/08/2016 07/08/2016 -
Téléchargé le
7 août 2016
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Hypertension NCT00151775
Eligibility Hypertension NCT00151775
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Serious other conditions that could interfere with the analysis of the results or that could interfere with the well-being of the patient in the trial
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Description
Sensitivity to olmesartan medoxomil
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0386393
Description
prohibited medication
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0683610
Description
Caffeine consumption
Type de données
boolean
Alias
- UMLS CUI [1]
- C0948365
Description
Malignant hypertension
Type de données
boolean
Alias
- UMLS CUI [1]
- C0020540
Description
congestive heart failure, cardiomyopathy, or obstructive valve disease
Type de données
boolean
Alias
- UMLS CUI [1]
- C0018802
- UMLS CUI [2]
- C0878544
- UMLS CUI [3,1]
- C0018824
- UMLS CUI [3,2]
- C0549186
Description
Renal transplant
Type de données
boolean
Alias
- UMLS CUI [1]
- C0022671
Description
Nephritic syndrome
Type de données
boolean
Alias
- UMLS CUI [1]
- C0268732
Similar models
Eligibility Hypertension NCT00151775
- StudyEvent: Eligibility
C0019196 (UMLS CUI [2])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0386393 (UMLS CUI [1,2])
C0683610 (UMLS CUI [1,2])
C0878544 (UMLS CUI [2])
C0018824 (UMLS CUI [3,1])
C0549186 (UMLS CUI [3,2])