Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05996120

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

Led by University of Leicester · Updated on 2025-04-03

100

Participants Needed

11

Research Sites

88 weeks

Total Duration

On this page

Sponsors

U

University of Leicester

Lead Sponsor

N

NHS National Waiting Times Centre Board

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (18 years or older) scheduled for coronary artery bypass surgery and/or valve replacement/repair, either elective or urgent
  • European System for Cardiac Operative Risk Evaluation (EuroSCORE) II of 2 or higher
  • Able to understand and communicate to provide informed consent
  • Able to read and understand the English language
Not Eligible

You will not qualify if you...

  • Undergoing coronary artery bypass surgery combined with procedures requiring deep hypothermic arrest
  • Undergoing emergency or salvage surgery
  • Undergoing off-pump cardiac surgery
  • Participating in another interventional trial
  • Unable to provide informed consent

AI-Screening

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Trial Site Locations

Total: 11 locations

1

Glenfield Hospital, University Hospitals of Leicester NHS Trust

Leicester, Leicestershire, United Kingdom, LE3 9QP

Actively Recruiting

2

Blackpool Victoria Hospital, Blackpool Teaching Hospitals NHS Foundation Trust

Blackpool, United Kingdom, FY3 8NR

Not Yet Recruiting

3

University Hospitals Bristol and Weston NHS Foundation Trust

Bristol, United Kingdom, BS1 3NU

Actively Recruiting

4

Castle Hill Hospital, Hull University Teaching Hospitals NHS Trust

Cottingham, United Kingdom, HU16 5JQ

Actively Recruiting

5

Golden Jubilee National Hospital, NHS Golden Jubilee

Glasgow, United Kingdom, G81 4DY

Actively Recruiting

6

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

London, United Kingdom, SE5 9RS

Actively Recruiting

7

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

London, United Kingdom, SW3 6NP

Not Yet Recruiting

8

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

London, United Kingdom, UB9 6JH

Not Yet Recruiting

9

John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust

Oxford, United Kingdom, OX3 9DU

Actively Recruiting

10

Derriford Hospital, Plymouth University Hospitals NHS Trust

Plymouth, United Kingdom, PL6 8DH

Actively Recruiting

11

Northern General Hospital, Sheffield Teaching Hospitals NHS Foundation Trust

Sheffield, United Kingdom, S5 7AU

Actively Recruiting

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Research Team

G

Gavin J Murphy, FRCS, MD, MBChB, BSc

CONTACT

A

Ann Cheng, MBChB, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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