Study on Optimal Temperature During Cardiopulmonary Bypass (THERMIC-4)

Last updated: March 31, 2025
Sponsor: University of Leicester
Overall Status: Active - Recruiting

Phase

N/A

Condition

Coronary Artery Disease

Thrombosis

Congestive Heart Failure

Treatment

Hypothermic Cardiopulmonary Bypass

Normothermic Cardiopulmonary Bypass

Clinical Study ID

NCT05996120
0910
IRAS
  • Ages > 18
  • All Genders

Study Summary

In order to perform heart surgery, a machine called cardiopulmonary bypass (CPB), or more commonly known as a heart-lung machine, is used to maintain the circulation of oxygenated blood needed by the rest of the body and its organs.

Historically, when a patient is connected to CPB, their body is cooled below the normal body temperature. This is known as hypothermia. This is because scientific studies have previously shown that reduced body temperature lowers metabolism and therefore offers more protection to the brain and other organs due to the reduced oxygen requirement. The evidence supporting this practice, however, has been challenged throughout the history of cardiac surgery, with studies supporting that normothermia, or normal body temperature, is a safe alternative. Despite this, the practice of hypothermia has persisted. Published data from a survey of 139 cardiac surgeons in the United Kingdom showed that 84% still routinely employ hypothermic CPB during surgery.

To assess whether normothermic or hypothermic CPB is safer, a clinical trial requiring a large sample size and high recruitment rates will be required. Therefore, the investigators aim to assess firstly the feasibility of trial recruitment and allocation adherence in this study. 100 adults across 10 different cardiac surgery centres in the United Kingdom will be recruited to a multicentre feasibility randomised controlled trial comparing normothermia (active comparator) against hypothermia (control comparator) during cardiopulmonary bypass in cardiac surgery. This study will also test the ability of the Cardiothoracic Interdisciplinary Research Network (CIRN), a trainee-led research collaborative, to collect pilot data on Major Adverse Cardiac and Cerebrovascular Events (MACCE) using a regulation-approved electronic application HealthBitⓇ. Participants will also be asked to complete quality of life surveys. The results of this study will subsequently inform a large, adequately powered randomised controlled trial for optimal temperature management during CPB.

Eligibility Criteria

Inclusion

INCLUSION CRITERIA

Participants may enter the trial if all of the following apply

  1. Adult patients (≥ 18 years) scheduled for coronary artery bypass surgery and/or valve replacement/ repair, either in the elective or urgent setting.

  2. European System for Cardiac Operative Risk Evaluation (EuroSCORE) II of 2 or higher.

  3. Able to understand and communicate to provide informed consent.

  4. Able to read and understand the English language.

EXCLUSION CRITERIA

Participants may not enter the trial if any of the following apply:

  1. Patients undergoing coronary artery bypass surgery in combination with other procedures including cardiac or vascular procedures that require deep hypothermic arrest.

  2. Patients undergoing emergency or salvage surgery.

  3. Patients undergoing off-pump cardiac surgery.

  4. Patients who are participating in another interventional trial.

  5. Unable to provide informed consent.

Study Design

Total Participants: 100
Treatment Group(s): 2
Primary Treatment: Hypothermic Cardiopulmonary Bypass
Phase:
Study Start date:
May 20, 2024
Estimated Completion Date:
February 28, 2026

Study Description

Primary Objective

To assess the feasibility of trial recruitment and delivery to target in the United Kingdom of a multicentre randomised controlled trial on normothermia versus hypothermia during cardiopulmonary bypass in adult cardiac surgery.

Secondary Objective

To assess the feasibility of conducting a multicentre randomized controlled trial (RCT) using a novel Good Clinical Practice (GCP) approved remote data capture as the primary trial database alongside analysis of routinely collected healthcare data.

To obtain pilot data, undertaken by the Cardiothoracic Interdisciplinary Research Network (CIRN), to inform a subsequent large, adequately powered RCT for optimal temperature management during CPB.

Connect with a study center

  • Glenfield Hospital, University Hospitals of Leicester NHS Trust

    Leicester, Leicestershire LE3 9QP
    United Kingdom

    Active - Recruiting

  • University Hospitals of Leicester NHS Trust

    Leicester, Leicestershire LE3 9QP
    United Kingdom

    Active - Recruiting

  • Blackpool Victoria Hospital, Blackpool Teaching Hospitals NHS Foundation Trust

    Blackpool, FY3 8NR
    United Kingdom

    Site Not Available

  • University Hospitals Bristol and Weston NHS Foundation Trust

    Bristol, BS1 3NU
    United Kingdom

    Active - Recruiting

  • Castle Hill Hospital, Hull University Teaching Hospitals NHS Trust

    Cottingham, HU16 5JQ
    United Kingdom

    Active - Recruiting

  • Golden Jubilee National Hospital, NHS Golden Jubilee

    Glasgow, G81 4DY
    United Kingdom

    Active - Recruiting

  • Harefield Hospital, Guy's and St Thomas' NHS Foundation Trust

    London, UB9 6JH
    United Kingdom

    Site Not Available

  • King's College Hospital, King's College Hospital NHS Foundation Trust

    London, SE5 9RS
    United Kingdom

    Active - Recruiting

  • Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust

    London, SW3 6NP
    United Kingdom

    Site Not Available

  • John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust

    Oxford, OX3 9DU
    United Kingdom

    Active - Recruiting

  • Derriford Hospital, Plymouth University Hospitals NHS Trust

    Plymouth, PL6 8DH
    United Kingdom

    Active - Recruiting

  • Northern General Hospital, Sheffield Teaching Hospitals NHS Foundation Trust

    Sheffield, S5 7AU
    United Kingdom

    Active - Recruiting

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