Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07181356

Effects of Long-term Remote Ischemic Preconditioning on Clinical Outcome in Patients With Acute Myocardial Infarction

Led by Henan Institute of Cardiovascular Epidemiology · Updated on 2025-09-18

2146

Participants Needed

1

Research Sites

204 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

At present, there are 290 million cardiovascular patients in China, including 11 million patients with coronary heart disease. Remote ischemic preconditioning(RIPC) may play an effective endogenous cardiac protection.This study will explore whether long-term use of RIPC in patients with AMI after PCI and non interventional therapy can reduce the incidence of major adverse cardiovascular cerebrovascular events(MACCE) and improve clinical outcomes and long-term prognosis.

CONDITIONS

Official Title

Effects of Long-term Remote Ischemic Preconditioning on Clinical Outcome in Patients With Acute Myocardial Infarction

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with acute myocardial infarction according to the Global Unified Definition of the Fourth Myocardial Infarction
Not Eligible

You will not qualify if you...

  • Patients who cannot tolerate remote ischemic preconditioning (RIPC) or RIPerC
  • Presence of aortic dissection, coronary artery aneurysm, coronary artery fistula, or other systemic organic diseases
  • Severe hypertension with uncontrolled systolic blood pressure over 180 mmHg or diastolic blood pressure over 120 mmHg
  • Severe liver dysfunction (bilirubin > 20 mmol/L, prothrombin time > 2.0 ratio)
  • Severe renal insufficiency (glomerular filtration rate < 30 ml/min/1.73 m2)
  • Current use of nicorandil or other drugs affecting microcirculation
  • Pregnancy

AI-Screening

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Trial Site Locations

Total: 1 location

1

Fuwai Central China Cardiovascular Hospital

Zhengzhou, Henan, China, 450000

Actively Recruiting

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Research Team

M

Muwei LI

CONTACT

G

GUO QUAN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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