Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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
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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