Cardiomyopathy Trial, Recruiting NCT06607471 Sponsor: Scientific Institute San Raffaele Condition: Cardiomyopathy
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Cardiomyopathy Trial, Recruiting

NCT06607471
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:

  • People who have given written agreement to take part (for children, a parent or guardian must provide this consent on their behalf, following the rules of the country where the trial takes place)
  • People who are suspected of having, have been diagnosed with, or have a genetic profile consistent with a non-ischaemic cardiomyopathy (a heart muscle condition not caused by blocked arteries) — this includes a wide range of heart muscle conditions such as dilated, thickened, or stiff heart muscle diseases, heart rhythm disorders with structural changes, pregnancy-related heart conditions, storage diseases, and many others

Who may not be able to join:

  • People who have not provided written agreement to take part
  • People who have been confirmed to have a heart condition caused by something other than a non-ischaemic cardiomyopathy
  • People who do not have enough test results or medical records available for the trial team to assess their heart condition, heart rhythms, or heart inflammation
  • People being enrolled based on past records who are no longer actively being followed up at the enrolling centre

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: Paolo Della Bella, MD, San Raffaele Scientific Institute, Milan, Italy

Phone: +39 0226437482

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

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Scientific Institute San Raffaele
Registry
ClinicalTrials.gov
Start date
30 January 2018
Est. completion
31 December 2035

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Assessment of diagnostic accuracy (in terms of true/false positive/negative rates) amongst different diagnostic techniques in DCM; Assessment of diagnostic accuracy (in terms of true/false positive/negative rates) amongst different diagnostic techniques in DCM; Assessment of diagnostic accuracy (in terms of true/false positive/negative rates) amongst different diagnostic techniques in DCM; Assessment of diagnostic accuracy (in terms of true/false positive/negative rates) amongst different diagnostic techniques in DCM; Assessment of diagnostic accuracy (in terms of true/false positive/negative...

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