Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT07068399

Use of Shock Wave Therapy for Neo-Vascularisation in Non-critical Coronary Artery Disease: Validation by Quantitative Cardiac MRI Perfusion

Led by The University of Hong Kong · Updated on 2025-07-16

100

Participants Needed

1

Research Sites

278 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a randomised controlled trial aimed to demonstrate the effect of cardiac extracorporeal shock wave therapy (CSWT) on the angiogenesis effect of myocardium by determining myocardial perfusion and left ventricular function in patients with coronary artery disease (CAD) when measured by cardiac MRI before and after the treatment.

CONDITIONS

Official Title

Use of Shock Wave Therapy for Neo-Vascularisation in Non-critical Coronary Artery Disease: Validation by Quantitative Cardiac MRI Perfusion

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with symptoms of coronary artery disease
  • Patients without obstructive coronary artery disease
  • Left ventricular ejection fraction (LVEF) not less than 40%
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Pregnancy or lactation
  • Contraindication to contrast-enhanced stress Cardiac Magnetic Resonance (e.g., estimated GFR <30ml/min/1.73m2, severe allergy to gadolinium-based contrast agent, contraindication to adenosine)
  • Life expectancy less than 24 months
  • Haemodynamically unstable
  • Participation in another clinical trial within 6 months of enrollment
  • Recent myocardial infarction within 6 months
  • Unable to consent to or perform study components

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

HKU Li Ka Shing Faculty of Medicine

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

M

Ming-Yen NG, BMBS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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