Heart Disease Trial, Recruiting NCT07449377 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Heart Disease
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Heart Disease Trial, Recruiting

NCT07449377
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:

  • You are 18 years old or older
  • You have come to the emergency department with sudden shortness of breath, and there is no other clear reason found for it (such as a collapsed lung, a new lung infection, a heart attack, or Covid-19)
  • You are affiliated with the French social security system (note: AME coverage does not qualify)
  • You have read the information about the trial and signed a consent form agreeing to take part

Who may not be able to join:

  • You have a known long-term liver condition, including liver scarring (fibrosis) or a blood clotting result that suggests serious liver problems
  • You have any open wounds or skin damage on your abdomen (belly area) where the liver scan device would be used
  • You have previously had a liver transplant
  • Your kidneys are not working well enough (based on a specific kidney function measurement — confirm with trial site)
  • You are under a legal guardianship or protection order, or you are not free to make your own decisions (such as being in custody)
  • You are currently pregnant or breastfeeding
  • You are already taking part in another clinical trial that involves an intervention or treatment

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: Amélie VROMANT, Medical Doctor, Assistance Publique - Hôpitaux de Paris

Phone: +33617253512

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
Registry
ClinicalTrials.gov
Start date
2 April 2026
Est. completion
1 November 2026

Where this trial is recruiting

🇫🇷 France

Primary endpoints

The Area under the Receiving Operator Characteristic curve (AUC ROC) of Liver Stiffness Measurement (LSM) value to diagnose AHF. Other diagnostic performances will also be assessed at the threshold determined by Youden's method.

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