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NCT07632027Not yet recruiting

Bedside Assessment of Right Ventricular Output Lying in Prone Or Supine

Bedside Assessment of Right Ventricular Output Lying in Prone Or Supine (the BAROLO Study) Hemodynamic Changes Due to Prone Position in Patients After Cardiac Surgery - a Prospective Randomized Controlled Trial Evaluating the Effect of Prone Position on Right Heart Function

Source: ClinicalTrials.gov · Last updated 23 Oct 2026

Brief summary (registry, in English)

Right ventricular failure (RVF) is a common complication to cardiac surgery, which is associated to mortality, kidney failure, stroke, prolonged mechanical ventilation and ICU stay. The right ventricle is particularly vulnerable to an increased afterload. By increasing pulmonary vascular resistance (PVR), atelectasis might mitigate a negative effect on the right ventricle. Recruitment maneuvers have been shown to resolve atelectasis and improve hemodynamics by increasing cardiac output and lowering PVR. However these maneuvers transiently raise airway pressures, which in turn increases right ventricular afterload, a situation often poorly tolerated by patients with RVF. Prone position is used in patients with respiratory failure and has been shown to decrease mortality in patients with ARDS. Prone position decreases atelectasis and moves ventilation dorsally. In ARDS it also seems to mediate beneficial hemodynamic effects such as an increase in cardiac output and a decrease in PVR. The investigators hypothesis is that prone position early after cardiac surgery will increase cardiac output by recruitment of atelectasis and thereby decrease PVR.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
70 (estimated)
First submitted
24 Mar 2026
Start date
Oct 2026
Primary completion date
May 2029
Lead sponsor
Sahlgrenska University Hospital
NCT number
NCT07632027

What you commit to

  • Study type: Interventional
  • Planned participants: 70
  • From Oct 2026 to the primary completion date, May 2029
  • 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.

Prior treatment

  • Emergency surgery

Other illness

  • Severe pulmonary disease
  • Any condition which, in the judgement of the investigator, might increase the risk to the patient

Other

  • BMI \>40
  • Haemodynamic instability requiring Norepinephrine \>0.5mcg/kg/min
  • Intracardiac shunt
  • Severe (or worse) tricuspid regurgitation

Who the study is looking for

  • Scheduled for cardiac surgery using cardiopulmonary bypass

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
Cardiothoracic Intensive Care Unit
Coordinator of this site? Confirm its status
GothenburgSwedenUnknown status

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