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Clinical Trials/NCT06616233
NCT06616233RecruitingNot Applicable

Effects of Chronic Remote Ischaemic Conditioning on Coronary and Peripheral Vascular Function in Patients With Heart Failure

University of Leicester1 site in 1 country60 target enrollmentStarted: April 8, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Myocardial perfusion reserve

Study Overview

Brief Summary

This study will test the impact of remote ischaemic conditioning combined with exercise on myocardial perfusion in patients with or at risk of heart failure

Detailed Description

Heart failure (HF) is a disease which affects the heart's ability to pump or fill with blood. It can affect a person's quality of life and their ability to exercise. Recent work has shown that a reduction in the blood supply to the heart may contribute to the problem. It is therefore possible that improving the blood supply to the heart may help patients with HF. One possible way that this might be achieved is with a method called remote ischaemic conditioning (RIC). This involves placing a cuff on a person's arm (identical to a blood pressure cuff) and inflating it for a few minutes to reduce the blood flow in a person's arm. This is thought to release chemicals into the bloodstream which can have positive effects on the heart. This has been studied in patients with other forms of heart disease, but is yet to be tested properly in patients with heart failure. It is hypothesized that combining the RIC procedure with a low level of arm exercise may result in further improvements in the person's blood vessels and heart. This will be tested in a single-centre prospective study.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Masking Description

Blinded analysis of data

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age >18 years
  • •Ability to provide written consent
  • •clinical diagnosis of HFpEF (LVEF ≥50%; symptoms and signs of heart failure [HF] caused by a structural and/or functional abnormality, and at least one: elevated natriuretic peptides; ambulatory; BNP ≥35 pg/mL or NT-proBNP ≥125 pg/mL or hospitalised; BNP ≥100 pg/mL or NT-proBNP ≥300 pg/mL, and objective evidence of cardiogenic pulmonary or systemic congestion) OR stable type 2 diabetes (determined by formal diagnosis in hospital or GP case records with diagnostic oral glucose tolerance test or glycated haemoglobin level ≥6.5%) and with ACC/AHA stage B HF (structural disorder of the heart but no current or previous symptoms of HF) OR confirmed diagnosis of dilated cardiomyopathy

Exclusion Criteria

  • •Absolute contraindications to MRI or contrast (e.g. severe claustrophobia, pregnancy, ferromagnetic implants, inability to lie flat, severe renal impairment eGFR<30ml/min/m2)
  • •Moderate to severe valvular heart disease
  • •Confirmed coronary artery disease (>50% narrowing in any major epicardial coronary artery on invasive or computed tomography coronary angiography, previous myocardial infarction, previous percutaneous intervention or coronary bypass surgery)
  • •Known arterial stenosis of the upper extremity

Arms & Interventions

Remote Ischaemic Conditioning with Exercise

Experimental

Participants will be randomised to receive remote ischaemic conditioning (RIC) with exercise involving a 4-week home-based programme of RIC with exercise . The exercise will involve handgrip exercise during the cuff deflation phase of RIC.

Intervention: Remote Ischaemic Conditioning with exercise (Device)

Remote Ischaemic Conditioning

Other

Participants will receive remote ischaemic conditioning (RIC) without exercise involving a 4-week home-based programme of RIC.

Intervention: Other: Remote Ischaemic Conditioning (Device)

Outcomes

Primary Outcomes

Myocardial perfusion reserve

Time Frame: 4 weeks

myocardial perfusion reserve under adenosine stress as assessed by quantitative cardiovascular magnetic resonance (CMR)

Contraction strength in the cuff deflation phase of RIC

Time Frame: 1 day

contraction force achieved during cuff deflation phase, measured in Newtons

Hyperaemic myocardial blood flow

Time Frame: 4 weeks

myocardial blood flow under adenosine stress as assessed by quantitative cardiovascular magnetic resonance (CMR)

Secondary Outcomes

  • Cardiopulmonary exercise test(4 weeks)
  • Brachial artery flow mediated dilation(4 weeks)
  • Skeletal muscle strength(4 weeks)
  • Skeletal muscle endurance(4 weeks)
  • Brachial artery maximal dilatory capacity(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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