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Clinical Trials/NCT01128790
NCT01128790CompletedNot Applicable

Effect of Remote Ischemic Preconditioning on Exercise Capacity in Patients With Heart Failure: A Double Blind Randomized Control Trial

University Health Network, Toronto1 site in 1 country22 target enrollmentStarted: October 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
22
Locations
1
Primary Endpoint
Exercise performance - VO2, exercise time, exercise workload, anaerobic threshold

Study Overview

Brief Summary

The purpose of this study is to determine the effect of remote ischemic preconditioning on exercise capacity in patients with heart failure.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • LV ejection fraction <40%
  • NYHA functional class II-IV
  • Non ischemic cardiomyopathy

Exclusion Criteria

  • recent cardiovascular hospitalization (within last 4 weeks)
  • ischemic cardiomyopathy
  • diabetes mellitus
  • peripheral neuropathy
  • ventricular assist device
  • contraindications to exercise stress testing

Arms & Interventions

remote ischemic preconditioning

Experimental

4 cycles of 5 mins upper limb ischemia induced by blood pressure cuff inflation 20mmHg above systolic blood pressure

Intervention: Remote ischemic preconditioning (Other)

Sham control

Sham Comparator

4 x 5 mins of upper limb blood pressure cuff inflation to 10mmHg (non-occlusive)

Intervention: Sham Control (Other)

Outcomes

Primary Outcomes

Exercise performance - VO2, exercise time, exercise workload, anaerobic threshold

Time Frame: 1 week

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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