Cardiomyopathy Trial, Recruiting NCT05888662 Sponsor: Rennes University Hospital Condition: Cardiomyopathy
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Cardiomyopathy Trial, Recruiting

NCT05888662
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 years or older
  • People undergoing their first radiofrequency ablation procedure for a type of irregular heartbeat (ventricular tachycardia) caused by ischaemic heart disease (reduced blood flow to the heart)
  • People who have an implanted defibrillator (ICD) with remote monitoring capability
  • Women who could become pregnant must be using effective contraception until they leave the hospital
  • People who have given written consent to participate freely and without pressure
  • People who have health insurance or are covered by a health fund

Who may not be able to join:

  • People who have had certain types of heart surgery in the past (such as bypass surgery, heart valve replacement, or other operations that may have caused scar tissue around the heart) that could make one part of the procedure unsafe
  • People found to have a blood clot inside the left side of the heart during pre-procedure scans
  • People taking blood-thinning medication that cannot be safely paused for the procedure
  • People taking two types of blood-thinning tablet together, where it is not possible to temporarily reduce this to just one
  • People with a history of inflammation of the sac surrounding the heart (pericarditis)
  • People who have previously had radiotherapy to the chest area
  • People for whom general anaesthesia is not safe
  • People who are pregnant or breastfeeding
  • People who have previously had a serious reaction to heparin, a blood-thinning medication used during the procedure (confirm with trial site)
  • People who are under legal protection orders, have restricted legal capacity, are not free to make their own decisions, or are unable to give informed consent

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 28 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: Raphaël MARTINS, MD, PhD, Rennes University Hospital

Phone: 299282517

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
Rennes University Hospital
Registry
ClinicalTrials.gov
Start date
23 October 2023
Est. completion
23 October 2029

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Survival free from ventricular arrhythmia recurrence

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: 28 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