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Clinical Trials/NL-OMON37928
NL-OMON37928
Completed
N/A

High Intensity Interval Training after Cardiac Resynchronization Therapy: a randomised controlled trial - HIT-CRT

Maxima Medisch Centrum0 sites60 target enrollmentTBD
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ConditionsCardiac Resynchronization TherapyChronic Heart Failure10019280

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cardiac Resynchronization Therapy
Sponsor
Maxima Medisch Centrum
Enrollment
60
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Maxima Medisch Centrum

Eligibility Criteria

Inclusion Criteria

  • •\-Written informed consent.
  • •\-Systolic heart failure due to ischemic cardiomyopathy (due to one or more myocardial infarction, as confirmed with echocardiography) or dilating cardiomyopathy (no history of myocardial infarction, no proven ischemia, no congenital heart disease and no severe valve disorder)
  • •\-Left ventricular ejection fraction \< 35% before CRT.
  • •\- New York Heart Association (NYHA) classII or III before CRT

Exclusion Criteria

  • •\* Myocardial infarction or unstable angina less than 3 months prior to inclusion
  • •\* Clinical signs of decompensated heart failure
  • •\* Ventricular tachycardia or ischemia during exercise
  • •\* Participation in a training program (\*2/week) in the last year
  • •\* Intracardiac shunts or congenital heart disease limiting exercise capacity
  • •\* Orthopaedic, vascular, pulmonary, neuromuscular and other disease limiting exercise capacity
  • •\* Pathological Allen test , In casu no sufficient collateral circulation to the hand, in case of radial artery cannulation.

Outcomes

Primary Outcomes

Not specified

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