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Clinical Trials/NCT00690209
NCT00690209
Completed
Phase 2

Efficacy of Surgical Coronary Revascularization Associated With Stem Cells Injection in Patients With Severe Chronic Ischemic Heart Disease With Residual Viability. A Prospective, Controlled Pilot Trial.

University Hospital, Clermont-Ferrand1 site in 1 country12 target enrollmentMay 2008

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Ischemic Heart Disease
Sponsor
University Hospital, Clermont-Ferrand
Enrollment
12
Locations
1
Primary Endpoint
Evolution of left ventricular volumes and contractility Evolution of left ventricular volumes and contractility
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Surgical revascularization has proven its efficacy in term of morbidity and mortality in patients with multivessel coronary disease and poor left ventricular function. Nevertheless, if left ventricle is severely dilated, the improvement of global contractility and reduction of volumes is frequently absent after CABG even if substantial amount of myocardial viability is present. A value of > 140 ml for end systolic volume has been proposed as the cut off for the absence of recovery after revascularization.

Recently, a reduction of cardiac volumes and improvement of regional and global contractility has been demonstrated in patients with advanced ischemic heart disease, severe dilation of left ventricle and poor candidates for revascularization after injection of stem cells in territories with residual viability.

Detailed Description

The screening of patients will be performed after contrast coronar ventriculography realized for diagnostic or prognostic purpose. Subsequently all patients will be evaluated by cardiac ce-MR and PET imaging for verification of inclusion criteria. Patients will be allocated in a single blind manner to one of two therapeutic arms: surgical revascularization alone or surgical revascularization associated with autologous bone marrow derived stem cells injection in viable territories. During the follow up evolution of left ventricular volumes and contractility will be analyzed by ce-MR and PET imaging at 1 year. Additionally patients' functional status will be assessed by metabolic stress tests and quality of life questionnaire at 6 months, 1 year and 2 years.

Registry
clinicaltrials.gov
Start Date
May 2008
End Date
January 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Clermont-Ferrand
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Chronic ischemic heart disease
  • Left ventricular dilation (end systolic volume \>140 ml)
  • Poor global contractile function (ejection fraction \<40%)
  • Substantial amount of residual viability (\>30% of left ventricle)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Evolution of left ventricular volumes and contractility Evolution of left ventricular volumes and contractility

Secondary Outcomes

  • Functional status

Study Sites (1)

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