ISRCTN ISRCTN72268178
DOI https://doi.org/10.1186/ISRCTN72268178
Protocol serial number N/A
Sponsor Sponsor not defined - Record provided by the Medical Research Council (UK)
Funder Medical Research Council (UK)
Submission date
07/09/2005
Registration date
08/09/2005
Last edited
19/05/2011
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Circulatory System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Tom Meade
Scientific

Non-communicable Disease Epidemiology Unit
London School of Hygiene and Tropical Medicine
Keppel Street
London
WC1E 7HT
United Kingdom

Email tom.meade@lshtm.ac.uk

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Scientific title
Study objectivesLowering mild to moderate hypertension leads to a reduction in rates of stroke, deaths due to hypertension and of coronary events in men and women aged 35-64 years.
Ethics approval(s)Not provided at time of registration.
Health condition(s) or problem(s) studiedHypertension
InterventionBendrofluazide or propranolol compared with placebo.
Intervention typeDrug
PhaseNot Specified
Drug / device / biological / vaccine name(s)Bendrofluazide and propranolol
Primary outcome measure(s)

Stroke, deaths due to hypertension and of coronary events.

Key secondary outcome measure(s)

Not provided at time of registration

Completion date01/12/1982

Eligibility

Participant type(s)Patient
Age groupAdult
SexAll
Target sample size at registration18000
Key inclusion criteriaMen and women age 35-64 at recruitment in 176 general practices in the Medical Research Council's General Practice Research Framework. Diastolic blood pressure of 90-109 mmHg with a systolic pressure below 200 mmHg.
Key exclusion criteriaSecondary hypertension; already on antihypertensive treatment; accepted indication for antihypertensive treatment; myocardial infarction or stroke within previous three months; presence of angina, intermittent claudication, diabetes, gout, bronchial asthma, serious intercurrent disease, pregnancy.
Date of first enrolment01/01/1973
Date of final enrolment01/12/1982

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Non-communicable Disease Epidemiology Unit
London
WC1E 7HT
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 15/02/1992 Yes No