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Clinical Trials/NCT01214499
NCT01214499
Unknown
Phase 2

Prospective, Controlled and Randomized Clinical Trial on Cardiac Cell Regeneration With Laser and Autologous Bone Marrow Stem Cells, in Patients With Coronary Disease and Refractory Angina

Fundación de Investigación Biomédica - Hospital Universitario de La Princesa1 site in 1 country20 target enrollmentOctober 2010

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Angina
Sponsor
Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
Enrollment
20
Locations
1
Primary Endpoint
New York Heart Association (NYHA)classification for angina
Last Updated
15 years ago

Overview

Brief Summary

Coronary disease is one of the most frequent pathology of the modern world and the leading cause of death in the investigators country. In Spain more than 50.000 coronary percutaneous intervention and more than 5.000 coronary artery bypass graft (CABG) procedures are performed every year. Despite this data about 12% of patients have diffuse coronary disease and are not candidates to conventional therapies. Also between 15-25% of patients undergoing coronary bypass grafting receive an incomplete revascularization due to the poor quality of the coronary vessels.

Transmyocardial revascularization (TMR) is a surgical procedure that uses a laser to create channels through the myocardial, so this laser stimulates local angiogenesis and provides blood in the ischemic area. Results of this procedure have shown clear benefits in terms of reduction of angina and increase of survival of patients, compared to medical treatment.

Cell therapy in heart disease is offering in recent years encouraging results despite the methodological difficulties that being able to use this technique sometimes involves. The basis lies in the potential ability of stem cells to differentiate into any type of adult cell. In the case of cardiac cell therapy, stem cells can differentiate into myocardial cells or vascular cells capable of developing angiogenesis. Further studies are needed to draw firm conclusions about the clinical impact that the use of stem cells has on cardiovascular disease.

Recently a system has been developed to create, at the same time and in a simple and effective way, the laser channels and the introduction of stem cells on the edges of these channels. This system called PHOENIX ™ consists of a laser probe capable of creating transmural channels in the myocardium.

Based on the what has just been explained, it is quite possible that the combination of both therapies can increase successful results regarding the reduction in angina these patients need. Initially, and after having some experience with this type of treatment, the results could be analyzed and compared with the results obtained through laser therapy, with the help of a controlled clinical trial, such as the one the investigators are proposing.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
October 2012
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

Eligibility Criteria

Inclusion Criteria

  • Patients over 18 years of age.
  • Patients with at least one area of myocardial ischemia or chronic myocardial infarction of the left ventricle demonstrated by any imaging technique not amenable to conventional revascularization and angina refractory to medical treatment.
  • Ejection fraction\> 25% measured in the six months prior to the procedure.
  • Participants must be mentally competent to give consent for inclusion in the clinical trial

Exclusion Criteria

  • Patients with unstable angina defined as the need for intravenous nitrates at the time of surgery.
  • Recent myocardial infarction (within 15 days before the procedure).
  • Patients with decompensated heart failure at the time of surgery.
  • Severe or life threatening arrhythmia (ventricular tachycardia or fibrillation) in the week before the procedure.
  • Patients requiring some type of concomitant valvular surgery.
  • Patients with severe obstructive lung disease criteria who are considered as not capable of bearing general anesthesia

Outcomes

Primary Outcomes

New York Heart Association (NYHA)classification for angina

Time Frame: one year

The main variable under study is the percentage of patients achieving a decrease in two levels of the NYHA classification for angina.

Secondary Outcomes

  • The demographic, intra and postoperative variables(one year)
  • Tests(one year)
  • Quality of Life(one year)

Study Sites (1)

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