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Autologous Mesenchymal Stromal Cell Therapy in Heart Failure

A Single Centre, Randomised Controlled Study of the Effect of NOGA-guided Direct Intramyocardial Injection of Mesenchymal Stromal Cells on the Development of New Myocardium and Blood Vessels in Patients With Heart Failure

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00644410
Enrollment
59
Registered
2008-03-26
Start date
2008-09-30
Completion date
2015-03-31
Last updated
2015-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congestive Heart Failure

Keywords

heart failure, stem cell, mesenchymal stromal cell, mesenchymal stem cell

Brief summary

It is a single centre, randomised controlled study of the effect of NOGA-guided direct intramyocardial injection of mesenchymal stromal cells on the development of new myocardium and blood vessels in patients with heart failure. Stem cells will be obtained from the bone marrow and culture expanded for 6 - 8 weeks before injected into the myocardium. The patients will be followed with safety, clinical, MRI and CT endpoints for 1 year.

Detailed description

The primary objective is to investigate the regenerative capacity of direct intra-myocardial injection of mesenchymal stromal cells in patients with reduced left ventricular EF (≤45%) and heart failure NYHA 2-3. A total of 60 patients with will be enrolled in the study and randomised 2: 1 to cells or placebo (saline). The patients will be followed for 12 months. The primary endpoint is changes in left ventricle end-systolic volume (LVESV) at 6 months follow-up. The secondary endpoints are changes in left ventricular ejection fraction (LVEF), end-diastolic volume and end-systolic mass at 6 months follow-up. Other secondary endpoints are NYHA, CCS, Kansas City Cardiomyopathy Questionnaire (KCCQ), 6 min walking test, and major adverse events endpoints: all-causes death, cardiovascular death, and hospitalization for worsening heart failure and MI at 12 months follow-up.

Interventions

BIOLOGICALMesenchymal stromal cell

Mesenchymal stromal cells 20 - 40 mill.

BIOLOGICALSaline

12 injection with 0.2 ml saline

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* EF \< 45 % * NYHA 2 - 3

Exclusion criteria

* Acute coronary syndrome within last 6 weeks. * Pregnancy * FEV1 \<1.0 * Cancer * Any severe disease which could interfere with the treatment or the outcome

Design outcomes

Primary

MeasureTime frame
Improvements in left ventricular function6 and 12 months

Secondary

MeasureTime frame
Clinical improvements6 and 12 months

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026