Congestive Heart Failure Clinical Trial
Official title:
Intra Cardiac Autologous Stem Cells Infusion May Improve Clinical Outcomes in Failing Heart Subjects Refractory to Maximal Drug Therapy and Internal Cardioverter With a Defibrillator (ICD) Recipients
NCT number | NCT02871466 |
Other study ID # | 8.2016 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | January 2010 |
Est. completion date | July 2022 |
stem cells therapy may be a choice therapy for advanced heart failure patients refractory to medical therapy, internal cardiovertor with a defibrillator (ICD) recipients, and a previous history of myocardial infarction and coronary artery revascularization. These patients, without indication to receive a cardiac resynchronization therapy (CRT), may have a worsening of heart failure, and symptoms of coronary artery disease. In this study we have evaluated in consecutive 30 selected patients the amelioration in failing heart NYHA class, hospitalization rate, echocardiographic left ventricle functionality, and associated to reduction of angina after a treatment with stem cells intra thoracic infusion.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | July 2022 |
Est. primary completion date | January 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - heart failure post coronary artery disease, refractory to maximal medical therapy, previous coronary artery surgical revascularization. Exclusion Criteria: - inflammatory chronic diseases, neoplastic diseases. |
Country | Name | City | State |
---|---|---|---|
Italy | Celestino Sardu | Naples | |
Italy | Raffaele Marfella | Naples | |
Italy | Celestino Sardu | Napoli |
Lead Sponsor | Collaborator |
---|---|
University of Campania "Luigi Vanvitelli" |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | NYHA class improvement | 12 months | ||
Primary | reduction in hospitalization rate | 12 months | ||
Primary | reduction in angor symptoms | 12 months |
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