Coronary Disease Clinical Trial
Official title:
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
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.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
Completed |
NCT05672862 -
International Post-PCI FFR Extended Registry
|
||
Completed |
NCT04492423 -
VerifyNow® PRUTest® Cardiovascular Population Expected Values On-Drug Study
|
||
Completed |
NCT01205776 -
EXCEL Clinical Trial
|
N/A | |
Recruiting |
NCT01218776 -
International Survey of Acute Coronary Syndromes in Transitional Countries
|
||
Completed |
NCT00046410 -
Comparison of the Risk of Stroke With On- Versus Off-Pump Coronary Artery Bypass Grafting
|
N/A | |
Recruiting |
NCT04390672 -
Multivessel TALENT
|
N/A | |
Not yet recruiting |
NCT02895009 -
Hemostatic Compression Patterns After Transradial Coronary Intervention
|
N/A | |
Completed |
NCT02784873 -
High Intensity Interval Training in UK Cardiac Rehabilitation Programmes
|
N/A | |
Completed |
NCT02948517 -
Time Restricted Feeding for Weight Loss and Cardio-protection
|
N/A | |
Recruiting |
NCT02859480 -
Dose-dependent Effect of Rosuvastatin on Long-term Clinical Outcomes After PCI
|
Phase 4 | |
Completed |
NCT02382731 -
Interventions to Support Long-Term Adherence aNd Decrease Cardiovascular Events Post-Myocardial Infarction
|
N/A | |
Completed |
NCT02510547 -
Comparison of a CrossBoss First Versus Standard Wire Escalation Strategy for Crossing Coronary Chronic Total Occlusion: the "CrossBoss First" Trial
|
Phase 4 | |
Withdrawn |
NCT02418143 -
A Study to Obtain Additional Information on the Use of CorMatrix® CanGaroo ECM® Envelope
|
||
Recruiting |
NCT01681381 -
Evaluate Safety And Effectiveness Of The Tivoli® DES and The Firebird2® DES For Treatment Coronary Revascularization
|
N/A | |
Completed |
NCT02248415 -
Administration of Warm Blood Cardioplegia With or Without Roller Pump
|
N/A | |
Recruiting |
NCT01207167 -
Mediators of Atherosclerosis in South Asians Living in America
|
||
Completed |
NCT02088138 -
Functional Electrical Stimulation in Cardiac Patients
|
N/A | |
Completed |
NCT02173067 -
Anesthesia With Epinephrine in Diabetes Patients is Safe and Effective
|
N/A | |
Completed |
NCT02133807 -
Specific Lp(a) Apheresis for Regression of Coronary and Carotid Atherosclerosis
|
Phase 3 |