ID
12973
Description
Efficacy and Safety of Chronic Administration of Telmisartan as Monotherapy or in Combination With Hydrochlorothiazide or Other Antihypertensive Medications in Patients With Mild to Moderate Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02177422
Lien
https://clinicaltrials.gov/show/NCT02177422
Mots-clés
Versions (1)
- 08/01/2016 08/01/2016 -
Détendeur de droits
CC BY-NC 3.0
Téléchargé le
8 janvier 2016
DOI
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Licence
Creative Commons BY-NC 3.0
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Eligibility Hypertension NCT02177422
Eligibility Hypertension NCT02177422
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
patients with a clinically significant change in ecg from baseline that was reported as an adverse event during the preceding clinical trial
Type de données
boolean
Alias
- UMLS CUI [1]
- C1623258
Description
patients who have developed a medical condition during the preceding clinical trial that, in the investigator's opinion, may be worsened by treatment or may compromise the safety evaluation of telmisartan
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2348563
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Description
patients who discontinued the preceding telmisartan clinical trial due to an adverse event
Type de données
boolean
Alias
- UMLS CUI [1]
- C2348568
Description
any other clinical condition which, in the opinion of the investigator, would not allow safe completion of the protocol and safe administration of telmisartan
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2348563
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Similar models
Eligibility Hypertension NCT02177422
- StudyEvent: Eligibility
C0248719 (UMLS CUI [2])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])