Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with 65 moderate mitral regurgitation during hospitalization
- Aged over 18 years
You will not qualify if you...
- Patients unable to provide written consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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