Can a new measuring ring make mitral valve repair more precise?
NCT ID NCT06965725
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This study tests a new paired-ring sizing tool used during mitral valve repair surgery. The tool measures the length of leaflet coaptation, which is how well the valve leaflets seal. Researchers want to see if this method gives accurate measurements compared to standard echocardiography. The study includes adults scheduled for mitral repair, and the tool is used only for observation, not to guide surgical decisions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A novel paired-ring sizing tool used once during mitral valve repair surgery, purely to measure leaflet coaptation length without influencing surgical decisions.
- What this could lead to
- If the sizing method proves accurate, it could help surgeons choose better ring sizes during mitral repair, potentially improving long-term valve function.
- What could go wrong
- This is a small, early study with 22 participants, so results may not apply broadly. The device is observational only, so it cannot directly improve outcomes, and measuring errors or imaging variability could limit conclusions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 22 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients undergoing mitral valve repair.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. All patients scheduled for mitral repair surgery 2. Age 18 years or older Exclusion Criteria: 1. Adults unable to consent, 2. Pregnant women and prisoners. 3. Emergency operations and those patients in whom mitral repair is not performed in a meaningful way, requiring mitral replacement instead, will be excluded. 4. Presence of acute endocarditis infection during the initial screening process
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Endeavor Health
RECRUITINGGlenview, Illinois, 60026, United States
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