Subacute Myocardial Infarction Clinical Trial
Official title:
An Open-label, Non-Randomized, Multi-Center Study to Assess the Safety and Cardiovascular Effects of Autologous ADSC Implantation by a Catheter Delivery System In Patients During the Subacute Recovery Phase of ST-Elevation MI
| Verified date | July 2017 |
| Source | Ageless Regenerative Institute |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The intent of this clinical study is to answer the questions: 1) Is the proposed treatment safe? and 2) Is treatment effective in improving cardiac function and clinical outcomes?
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | December 2018 |
| Est. primary completion date | September 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - Males and Females between Age 18 and 80 years. - Defined subacute myocardial infarction between 9-90 days from screening - Left ventricular ejection fraction at screening of = 50%, with 2 or more contiguous areas of severe wall motion abnormality on resting echocardiography. - Patients must have a minimum myocardial wall thickness of 5mm - Need or feasibility for re-vascularization has been ruled out by coronary angiogram or noninvasive stress testing. - Stable for at least 14 days on optimal medical management including: - Plavix/asprin therapy, anticoagulation therapy, cholesterol lowering agent, beta blocker, ACE inhibitor or ARB blocker Up to date on all age and gender appropriate cancer screening per American Cancer Society (Refer to section 9.3 for more details). Exclusion Criteria: - Females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study - Life expectancy < 6 months due to concomitant illnesses. - NYHA CHF Class 4 - Severe valvular or other non-ischemic myocardial disease. - Mechanical complications of the index acute myocardial infarction including but not limited to rupture of the mitral valve with resultant development of mitral regurgitation, rupture of the left ventricular free wall and rupture of the interventricular septum. - Previous severe reaction to radiocontrast agents - Exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study. - Serum creatinine > 2.5 mg/dL or end stage renal disease unless on dialysis. - Active infectious disease and/or known to have tested positive for HIV, HTLV, HBV, HCV, CMV (IgM > IgG) and/or syphilis. If the panel includes antibodies to the HBV-cAg and HBV-sAg, then an expert will be consulted as to patient eligibility based on the patient's infectious status - Any illness which, in the Investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results - Patients on chronic immunosuppressive transplant therapy - Systolic blood pressure (supine) =90 mmHg; - Resting heart rate > 100 bpm; - Active clinical infection within one week of enrollment. - Cerebrovascular accident within 6 months prior to study entry - Known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate. - History of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in the last five years. - Unwilling and/or not able to give written informed consent. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Ageless Regenerative Institute LLC | Aventura | Florida |
| Lead Sponsor | Collaborator |
|---|---|
| Ageless Regenerative Institute |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Improved cardiac function | Improvement is observed in cardiac function as assessed by echocardiographic LV function (EF) | 3 and 6 months after intervention | |
| Secondary | Adverse Event | The safety of adipose-derived stem cell injection will be evaluated by assessment of the frequency and nature of adverse events occurring during the study injection and up to the 6-month period following treatment. | Duration of study |