Skip to content

A clinical study for enhanced external counterpulsation combined with MSCs transplantation in the treatment of acute myocardial infarction

A clinical study for enhanced external counterpulsation combined with MSCs transplantation in the treatment of acute myocardial infarction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018788
Enrollment
Unknown
Registered
2018-10-09
Start date
2018-10-01
Completion date
Unknown
Last updated
2018-10-15

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

Conditions

acute myocardial infarction

Interventions

MSCs?::MSCs
EECP+MSCs???:EECP+MSCs

Sponsors

Jiangmen Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) aged 30 ~ 80 years old male and female; (2) for the first time, the anterior wall acute st-elevation myocardial infarction (STEMI) patients; (3) within 14 days of 24 hours and not the emergency opening infarction related coronary artery; (4) left ventricular overall low systolic function (LVEF 50% or less); (5) willing to stem cell therapy and follow-up examination within the given time; (6) have signed approved by the ethics committee of stem cell transplantation therapy of informed consent.

Exclusion criteria

Exclusion criteria: (1) the AMI complicated with cardiac shock (KILLIP4 level); (2) atrial fibrillation to warfarin anticoagulation or anticoagulant therapy at high risk of bleeding; (3) serious malignant arrhythmia (polymorphic ventricular tachycardia and ventricular fibrillation, ventricular flutter, height or III degree atrioventricular block need to implant a pacemaker); (4) the huge AMI complicated with left ventricular aneurysm requiring surgical operation; (5) with mechanical complications of acute myocardial infarction (including: ventricular septal perforation, papillary muscle rupture, etc.); (5) the AMI has line of stem cell therapy; (6) in chronic obstructive pulmonary disease (copd) (bronchial asthma, chronic bronchitis, emphysema, cor pulmonale); (7) of acute infectious diseases; (8) Hepatitis b, hepatitis c or AIDS patients; (9) blood system diseases, such as thrombocytopenia, severe anemia, leukemia, etc; (10) serious kidney disease, creatinine clearance 133 umol/L (11) liver function is abnormal obviously, GPT (ALT) > 3 times the upper limit of normal value; (12) has a history of cerebral hemorrhage patients; (13) in patients with malignant tumor; (14) cognitive dysfunction and dementia patients, patients with serious mental illness; (15) of patients with severe physical disabilities affect regular follow-up; (16) with some other serious uncontrolled system disease; (17) to prepare or have the pregnancy women patients; (18) have a PCI contraindications: such as digestive tract, intracranial and other parts of the patients at high risk of bleeding, or contrast allergy;Or intolerance to dual antiplatelet therapy for at least 1 year; (19) EECP contraindications to patients, to severe aortic regurgitation in full;Sandwich or aneurysm;Significant pulmonary hypertension; (20) unable or unwilling to sign the informed consent of the patients.

Design outcomes

Primary

MeasureTime frame
LVEF;LVDd;

Countries

China

Contacts

Public ContactWeidong Gao

Jiangmen Central Hospital

gaoweidong@medmail.com.cn+86 13652727518

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026