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Pilot Study of Remote Ischemic Preconditioning in Heart Failure

NCT01128790 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2013-12-23

No results posted yet for this study

Summary

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

Conditions

Interventions

OTHER

Remote ischemic preconditioning

4 cycles x 5 mins upper limb blood pressure cuff inflation 20mmHg above systolic blood pressure

OTHER

Sham Control

4 cycles x 5mins blood pressure cuff inflation to 10mmHg

Sponsors & Collaborators

  • The Hospital for Sick Children

    collaborator OTHER

  • University Health Network, Toronto

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01128790 on ClinicalTrials.gov