Actively Recruiting

Age: 45Years +
All Genders
ID06153563

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

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for mitral valve replacement
  • Age 45 years or older
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Surgery day

Participants undergo evaluation during mitral valve replacement surgery where tissue samples are collected for analysis.

1 visit (in-person, surgical procedure)

Long-term Monitoring

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

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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

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