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NCT05595954Recruiting

Impact of Personalised Cardiac Anaesthesia and Cerebral Autoregulation on Neurological Outcomes in Patients Undergoing Cardiac Surgery

Impact of Personalised Cardiac Anaesthesia and Cerebral Autoregulation on Neurological Outcomes in Patients Undergoing Cardiac Surgery (PRECISION)

Source: ClinicalTrials.gov · Last updated 30 Jun 2026

Brief summary (registry, in English)

This international, multicentre prospective cohort study will assess whether perioperative duration and magnitude of mean arterial pressure (MAP) outside of an individual's cerebral autoregulation (CA) limits using near-infrared spectroscopy (NIRS) and transcranial Doppler (TCD) are associated with adverse neurological events. It is to investigate whether patients with a higher burden of cerebral haemodynamic insults have an increased incidence or poorer neurological outcomes. Associations between neurologic outcomes, neurobiomarkers and genetic tests will be explored.

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
18 Oct 2022
Start date
23 Jan 2023
Primary completion date
4 May 2026
Lead sponsor
University Hospital, Basel, Switzerland
Diseases
Stroke
NCT number
NCT05595954

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 23 Jan 2023 to the primary completion date, 4 May 2026
  • 4 sites in 2 countries
  • 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

  • Surgery requiring moderate (28-31.9ºC) or deep (\<28ºC) hypothermic circulatory arrest;
  • Urgent (within 24 hours) and emergency surgery;

Other illness

  • Heart and/or lung transplantation;
  • Inability to give consent.
    • Participants who undergo cardiac surgery under minimal extracorporeal circulation will also be excluded.

Other

  • Inability to follow procedures or insufficient knowledge in English, German or French;

Who the study is looking for

  • Elective primary or reoperative coronary artery bypass graft and/or valvular and/or ascending aorta surgery requiring cardiopulmonary bypass.

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

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

SiteCityCountrySite status
Clinic for Anaesthesia, Intermediate Care, Prehospital Emergency Medicine and Pain Therapy, University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandCompleted
Inselspital, Bern University Hospital
Coordinator of this site? Confirm its status
BernSwitzerlandRecruiting
Cambridge University Hospitals and Brain Physics Lab
Coordinator of this site? Confirm its status
CambridgeUnited KingdomCompleted
Royal Papworth Hospital, Department of Anaesthesia and Intensive Care
Coordinator of this site? Confirm its status
CambridgeUnited KingdomCompleted

Related publications

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