Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
11 participants
INTERVENTIONAL
2004-04-30
2006-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
NONE
Interventions
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Enalapril 20 mg bd
Candesartan 8 mg bd
Eligibility Criteria
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Inclusion Criteria
* SBP 140-159 mmHg
* DBP 90-99 mmHg
Exclusion Criteria
* Pregnant or Breastfeeding
* Pre-menopausal women
* Uncontrolled cardiac or renal failure
* Diabetes mellitus
18 Years
70 Years
ALL
No
Sponsors
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St George's, University of London
OTHER
Principal Investigators
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Timothy WR Doulton, BSc MRCP
Role: PRINCIPAL_INVESTIGATOR
SGUL
Locations
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Blood Pressure Unit, Dept. Cardiac & Vascular Sciences, SGUL
London, , United Kingdom
Countries
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Other Identifiers
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LREC 01.87.10
Identifier Type: -
Identifier Source: org_study_id
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