Candesartan |
Atacand; candesartan cilexetil |
Clinical Trial: The Renin-Angiotensin System in Essential Hypertension
This study is currently recruiting patients.
Verified by St George''''s, University of London August 2005
|
Purpose
| Condition | Intervention |
|---|---|
| Hypertension | Drug: Enalapril 20 mg bd Drug: Candesartan 8 mg bd |
MedlinePlus related topics: High Blood Pressure
Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Open Label, Active Control, Crossover Assignment
Expected Total Enrollment: 11
Study start: April 2004; Expected completion: October 2006
Eligibility
Inclusion Criteria:
- Essential Hypertension
- SBP 140-159 mmHg
- DBP 90-99 mmHg
Exclusion Criteria:
- Intolerance of or allergy to ACE Inhibitors or ARBS
- Pregnant or Breastfeeding
- Pre-menopausal women
- Uncontrolled cardiac or renal failure
- Diabetes mellitus
Location and Contact Information
United Kingdom
Blood Pressure Unit, Dept. Cardiac & Vascular Sciences, SGUL, London, SW17 0RE, United Kingdom; Recruiting
Timothy WR Doulton, BSc MRCP, Principal Investigator
Timothy WR Doulton, BSc MRCP, Principal Investigator, SGUL
More Information
Last Updated: August 31, 2005
Record first received: August 31, 2005
ClinicalTrials.gov Identifier: NCT00141583
Health Authority: United Kingdom: Research Ethics Committee
ClinicalTrials.gov processed this record on 2005-09-06
Resources
- Atacand (Drug Digest)
- Atacand Consumer Information (U.S. Food and Drug Administration)

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