Heart Disease Trial, Recruiting NCT07131631 Sponsor: Minneapolis Heart Institute Foundation Condition: Heart Disease
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Heart Disease Trial, Recruiting

NCT07131631
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older who have heart failure where the heart's pumping function is weakened (specifically, the heart pumps out less than 50% of its blood with each beat, as measured by an ultrasound of the heart), and who have a leaky mitral valve (a valve in the heart) that is considered significant
  • People whose heart failure has already been treated as thoroughly as possible with medications and any relevant heart devices, following medical guidelines
  • People who are scheduled to have a minimally invasive procedure to repair the leaky mitral valve using an FDA-approved device called MitraClip

Who may not be able to join:

  • People who are having a heart artery procedure (called PCI) done at the same time as the mitral valve repair procedure
  • People who were born with a structural heart condition (congenital heart disease)
  • People whose heart failure is at the most advanced and severe stage (Stage D)
  • People with atrial fibrillation (an irregular heart rhythm) that is not under control
  • People who are pregnant
  • People who have more than a moderate leak in the tricuspid valve (another valve in the heart)
  • People who have more than a moderate leak or narrowing in the aortic valve (another valve in the heart)
  • People who have a medical reason they cannot undergo a cardiac MRI scan, or who are otherwise unable to have one (confirm with trial site)
  • People who have previously had repair or replacement surgery on their mitral valve

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 19 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: João Cavalcante, MD, Minneapolis Heart Institute Foundation

Phone: 612-863-3900

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Minneapolis Heart Institute Foundation
Registry
ClinicalTrials.gov
Start date
3 March 2022
Est. completion
1 July 2027

Where this trial is recruiting

🇮🇹 Italy 🇺🇸 United States

Primary endpoints

Estimate the association between LV myocardial fibrosis by CMR late gadolinium enhancement imaging before TEER with LV reverse remodeling.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov