Actively Recruiting

Age: 18Years +
All Genders
ID06876883

MItral Regurgitation Risk Assessment and CLinical modElling (MIRACLE Study)

Led by Sun Yat-sen University · Updated on 2025-09-05

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Mitral regurgitation (MR) is a common heart valve condition linked to higher risks of heart failure and death, especially if severe and untreated. MR can be classified as primary or secondary, and the study aims to understand risk factors for death or heart failure hospitalization in these patients. The MItral Regurgitation Risk Assessment and CLinical modElling (MIRACLE) study is a prospective cohort study enrolling adults diagnosed with moderate or worse MR during hospital stays to build a clinical model for guiding treatment decisions. Participants undergo thorough echocardiographic exams at the start to measure MR severity, heart function, and pulmonary artery pressure. The study observes these patients over an average of 5 years to collect data on their health outcomes. No treatments are assigned; instead, the study follows patients with MR to identify factors affecting their risk. During the study, participants' health will be monitored with ongoing assessments, focusing on all-cause death, cardiovascular death, and heart failure hospitalizations. The research team reviews these outcomes through the study completion, lasting about 5 years. The data collected aims to improve clinical decisions for managing MR and reducing adverse events.

CONDITIONS

Brief Title

MItral Regurgitation Risk Assessment and CLinical modElling

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with 65 moderate mitral regurgitation during hospitalization
  • Aged over 18 years
Not Eligible

You will not qualify if you...

  • Patients unable to provide written consent

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Approximately 5 years

Participants with moderate mitral regurgitation are observed over time to assess health outcomes including mortality and hospitalizations.

Trial Site Locations

Total: 1 location

1

The First Affiliated Hospital of Sun Yat-sen Univerity

Guangzhou, Guangdong, China, 510000

Actively Recruiting

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Research Team

X

Xiaodong Zhuang, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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