ID
12973
Beschrijving
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
Link
https://clinicaltrials.gov/show/NCT02177422
Trefwoorden
Versies (1)
- 08-01-16 08-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
8 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Hypertension NCT02177422
Eligibility Hypertension NCT02177422
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
patients with a clinically significant change in ecg from baseline that was reported as an adverse event during the preceding clinical trial
Datatype
boolean
Alias
- UMLS CUI [1]
- C1623258
Beschrijving
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
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2348563
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Beschrijving
patients who discontinued the preceding telmisartan clinical trial due to an adverse event
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
Beschrijving
any other clinical condition which, in the opinion of the investigator, would not allow safe completion of the protocol and safe administration of telmisartan
Datatype
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])