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NCT07163858Recruiting

Postural Mobilization Compared to Noradrenaline Only in Off-Pump CABG Surgery

Comparison of Hemodynamic Management by Postural Mobilization Versus Chemical Vasoconstriction Using Noradrenaline Exclusively in Off-pump Coronary Artery Bypass Graft Surgery: A Prospective, Randomized, Comparative, Single-center Study.

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

This interventional prospective randomized study is designed to compare hemodynamic management using postural mobilization (+/- noradrenaline) versus noradrenaline only in patients undergoing open-heart coronary artery bypass graft (CABG) surgery.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
1 Sept 2025
Start date
6 Oct 2025
Primary completion date
Jul 2027
Lead sponsor
Infirmerie Protestante de Lyon
NCT number
NCT07163858

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 6 Oct 2025 to the primary completion date, Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of cardiac surgery

Lab values

  • Renal failure (GFR \< 40 ml/min/1.73 m²)

Other

  • Contraindication to an inotropic substance (only NA will be used)
  • Contraindication to passive leg raising
  • Patient in a life-threatening emergency
  • Bilateral iliac or common femoral artery occlusion
  • EF \< 30%
  • Pregnancy and breastfeeding
  • Patient with bilateral thigh amputation
  • Class III obesity BMI \> 40 kg/m²

Who the study is looking for

  • Adult patient
  • patient requiring isolated coronary bypass surgery
  • Elective procedure or medical emergency
  • First cardiac surgery
  • Patient with an EF ≥30%
  • Mandatory affiliation to a social security system
  • Signed informed consent form
  • Suspension of renin-angiotensin system inhibitors and angiontensn-neprilysin receptor blockers and sartans the day before surgical procedure

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Infirmerie Protestante de Lyon
Coordinator of this site? Confirm its status
Caluire-et-CuireFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.