Heart Disease Trial, Recruiting NCT06973902 Sponsor: Quovadis Associazione Condition: Heart Disease
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Heart Disease Trial, Recruiting

NCT06973902
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 of any sex
  • People who are able to understand and sign a consent form agreeing to take part in the study and to allow their personal health data to be used
  • People living with heart failure that is still causing symptoms despite already receiving the best available medical treatment
  • People whose heart's left pumping chamber is not working at full strength (pumping less than 50% of its blood with each beat)
  • People who have been assessed by their doctors as suitable for a device called a Cardiac Contractility Modulation (CCM) implant, based on current European heart failure guidelines
  • People who have had at least one hospital admission, emergency department visit, or day hospital stay of more than 4 hours (for example, to receive heart medication through a drip) in the year before the implant

Who may not be able to join:

  • People whose life expectancy is less than 1 year due to serious health conditions unrelated to their heart
  • People for whom the CCM implant procedure is not medically suitable — for example, due to no usable blood vessel access, an active infection, a serious blood clotting disorder, or having a mechanical tricuspid heart valve
  • People who cannot safely undergo a stress echocardiogram (a heart scan performed with the help of medication) — reasons for this may include active heart failure, a recent heart attack, active heart or surrounding tissue inflammation, severe narrowing of the aortic heart valve, a tear in the main artery, serious uncontrolled heart rhythm problems, a known allergy to the medication used, or blood clots inside the heart chambers

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 21 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: Francesco Zanon, MD, UO Cardiologia, S. Maria della Misericordia Hospital, ULSS5 Polesana, Rovigo (I)

Phone: +39 049715373

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
Quovadis Associazione
Registry
ClinicalTrials.gov
Start date
10 July 2025
Est. completion
31 December 2028

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

New York Heart Association class variation

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: 21 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