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Clinical Trials/NCT00122811
NCT00122811
Unknown
Phase 4

The Hypertension in the Very Elderly Trial (HYVET)

Imperial College London7 sites in 6 countries4,000 target enrollmentNovember 2000

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Hypertension
Sponsor
Imperial College London
Enrollment
4000
Locations
7
Primary Endpoint
All strokes (fatal and non-fatal)
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to assess the benefits and risks of treating very elderly (those aged 80 or older) individuals with hypertension.

Detailed Description

The benefit to risk ratio of treating hypertensives aged 80 or older has not been established. It has been suggested that at this age for each stroke prevented there is one non-stroke death. HYVET is designed to help clarify this. HYVET is a randomised, double-blind, placebo-controlled trial in hypertensive subjects aged 80 or older. Active treatment consists of indapamide 1.5mg SR with the addition of perindopril 2mg - 4mg to reach a target blood pressure (BP) of \<150/80 mmHg. Entry criteria include a systolic blood pressure of 160-199 mmHg. Patients with isolated systolic hypertension (ISH) have been recruited since August 2003.

Registry
clinicaltrials.gov
Start Date
November 2000
End Date
October 2008
Last Updated
18 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Aged 80 or older
  • Sitting systolic BP 160-199 mmHg AND sitting diastolic BP \< 110 mmHg

Exclusion Criteria

  • Known accelerated hypertension (retinal haemorrhages or exudates or papilloedema).
  • Overt clinical congestive heart failure requiring treatment with a diuretic or angiotensin converting enzyme inhibitor. Subjects allowed if treated with digoxin only.
  • Renal failure (serum creatinine of more than 150 µmol/l).
  • Previous documented cerebral or subarachnoid haemorrhage in the last 6 months. (Ischaemic cerebral and cardiac events do not exclude, although the patient must be neurologically and cardiologically stable.)
  • Condition expected to severely limit survival, e.g. terminal illness.
  • Known secondary hypertension (e.g. renal artery stenosis, chronic renal insufficiency, and endocrine cause).
  • Clinical diagnosis of dementia.
  • Resident in a nursing home, i.e. where the dependency and care requirements of the patients are such that they require the regular input of qualified nurses and therefore the majority of staff in the home are nurses (other forms of residential care are acceptable).
  • Unable to stand up or walk
  • Participation in a drug trial within the past month preceding selection.

Outcomes

Primary Outcomes

All strokes (fatal and non-fatal)

Time Frame: Duration of trial

Secondary Outcomes

  • Stroke mortality(Duration of Trial)
  • Fracture rates(Duration of trial)
  • Cardiac mortality(Duration of trial)
  • Total mortality(duration of trial)
  • Cardiovascular mortality(Duration of trial)

Study Sites (7)

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