Heart Disease Trial, Recruiting NCT07163858 Sponsor: Infirmerie Protestante de Lyon Condition: Heart Disease
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Heart Disease Trial, Recruiting

NCT07163858
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 who need coronary bypass heart surgery (surgery to improve blood flow to the heart)
  • People having the surgery either as a planned procedure or as a medical emergency
  • People who have not had any previous heart surgery
  • People whose heart is pumping at a certain minimum level of strength (known as an ejection fraction of 30% or above)
  • People who are enrolled in a social security or health insurance system
  • People who have signed a consent form agreeing to take part
  • People who have stopped taking certain blood pressure medications (renin-angiotensin system inhibitors, angiotensin-neprilysin receptor blockers, and sartans) the day before the surgery

Who may not be able to join:

  • People for whom a certain type of medication used to support heart function (called an inotropic substance) is not safe to use
  • People for whom a technique called passive leg raising (gently lifting the legs to shift blood flow) is not appropriate
  • People in an immediately life-threatening emergency situation
  • People who have had heart surgery before
  • People who have a complete blockage in certain major arteries in the hips or upper legs (bilateral iliac or common femoral artery occlusion)
  • People whose heart pumping strength is below a certain level (ejection fraction below 30%)
  • People who are pregnant or breastfeeding
  • People with significant kidney problems (a kidney filtration rate below 40 ml/min/1.73 m²)
  • People who have had both legs amputated above the knee
  • People with a very high body weight classified as Class III obesity (BMI above 40 kg/m²)

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

Phone: +33 426297927

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
Infirmerie Protestante de Lyon
Registry
ClinicalTrials.gov
Start date
6 October 2025
Est. completion
1 July 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Assess use of noradrenaline in the experimental group (postural mobilization) vs control group (NA only) for hemodynamic management during open-heart coronary bypass graft surgery.

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