Actively Recruiting
Evaluation of the Elasticity of the Mitral Valve Chordae by Uniaxial Traction in Patients with Mitral Valve Regurgitation Comparing Mitral Valve Prolapse and Restriction of Mitral Valve Movement
Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2025-01-06
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the mechanobiological and histological properties of mitral valve chords in living humans, focusing on differences in elasticity between patients with mitral valve prolapse and those with restrictive ischemic mitral valve. This observational study addresses a gap in existing research, which primarily involves animal tissues or non-living human samples. The goal is to better understand mitral valve regurgitation through direct examination of living human tissue. The study will include 20 patients undergoing mitral valve replacement, selected consecutively without randomization. Tissue samples will be harvested during surgery and preserved in natural conditions without freezing to maintain their properties. Two groups are compared: one with mitral valve prolapse and the other with restrictive ischemic mitral valve movement. Data collection will include patient medical history and intraoperative results. Participants will be involved during their scheduled valve replacement surgery, when tissue samples are taken and analyzed. Researchers will measure the maximum value of Young's modulus to assess elasticity and perform initial histological evaluations of the tissue. The study aims to gather detailed mechanical and structural information on mitral valve chords, contributing to improved understanding of mitral valve disease. The total participation duration aligns with the surgical and data collection process.
CONDITIONS
Brief Title
Evaluation of the Elasticity of the Mitral Valve
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for mitral valve replacement
- Age 45 years or older
You will not qualify if you...
- Patients with mitral valve calcification
- Patients with rheumatic mitral valve disease
- Patients with mitral valve infections
- Patients who have had previous surgery on the mitral valve
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.
1 visit (in-person)
Duration - Surgery day
Participants undergo evaluation during mitral valve replacement surgery where tissue samples are collected for analysis.
1 visit (in-person, surgical procedure)
Duration - Up to 1 hour after tissue collection
Participants are observed following surgery with data collected on patient history and intraoperative results.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
CHU Saint-Etienne
Saint-Etienne, France, 42000
Actively Recruiting
Research Team
A
Andranik PETROSYAN, 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
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here