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Heart Revascularisation Trial - UK

Heart Revascularisation Trial - UK

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN66339600
Enrollment
140
Registered
2010-07-30
Start date
2003-03-07
Completion date
Unknown
Last updated
2019-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Cardiovascular

Interventions

1. Optimal medication plus angiography with, if appropriate, CABG 2. Optimal medication Follow-up length: 60 months Study entry: single randomisation o

Sponsors

Hull and East Yorkshire Hospitals NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Heart failure (in the investigators opinion) requiring chronic diuretic therapy 2. Coronary disease as the cause of heart failure as evidenced by a history of previous myocardial infarction, previous revascularisation or previous angiography 3. Left ventricular systolic dysfunction (ejection fraction less than 35%) 4. Stress-induced myocardial ischaemia or evidence of myocardial hibernation/stunning affecting five or more left ventricular segments in a 16-segment model 5. Male and female, lower age limit of 18 years

Exclusion criteria

Exclusion criteria: 1. Inability to give written informed consent. No age limits are stipulated but patients will have to be over 18 years to give consent and some patients may be considered too frail to survive surgery and would be excluded. 2. Patients who are not candidates for coronary artery bypass graft (CABG) surgery because of frailty or serious co-morbidity, e.g., severe lung disease, metastatic carcinoma. N.B. Some patients will be candidates for percutaneous transluminal coronary angioplasty (PTCA) but prior to randomisation (i.e. prior to doing an angiogram for study purposes) the investigator should be willing to send the patient to CABG surgery in case that is the preferred mode of revascularisation. 3. Unstable angina, myocardial infarction or stroke within the preceding 2 months 4. Patients being considered for revascularisation for the relief of chest pain (angina) or for valve surgery

Design outcomes

Primary

MeasureTime frame
Survival

Secondary

MeasureTime frame
Determine whether coronary revascularisation reduces all-cause and cause-specific hospitalisation

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026