MiR-181a: a potential biomarker of acute muscle wasting following elective high-risk cardiothoracic surgery.
Susannah A A Bloch, Anna V J Donaldson, Amy Lewis...
https://pubmed.ncbi.nlm.nih.gov/25888214Actively Recruiting
Led by Barts & The London NHS Trust · Updated on 2026-01-07
100
Participants Needed
1
Research Sites
N/A
Total Duration
B
Barts & The London NHS Trust
Lead Sponsor
Q
Queen Mary University of London
Collaborating Sponsor
Researchers are studying patients who have experienced severe cardiac or respiratory failure requiring life support with extracorporeal membrane oxygenation (ECMO) to understand recovery from intensive care unit-acquired weakness (ICUAW). This condition includes muscle and nerve damage that occurs in critically ill patients and can affect physical function and quality of life after hospital treatment. The study aims to identify factors influencing recovery and the impact of ICUAW on health-related quality of life (HRQoL) following critical illness. The study observes physical and psychological effects of ICUAW in patients receiving ECMO. Researchers will use ultrasound to measure the size of a leg muscle (Rectus Femoris cross-sectional area) during the first week of admission and at set times later. Muscle strength, physical performance tests, and quality of life questionnaires will be used to see how muscle size relates to recovery. Blood and urine samples will be collected to study molecular and genomic markers, and muscle biopsies may be taken when patients have surgery to start ECMO. Participants will be monitored up to about one year after their illness. Measurements include muscle strength tests, lung function, body composition, and questionnaires assessing anxiety, depression, and daily living reintegration. Biological samples will help understand molecular changes. This comprehensive approach aims to connect physical recovery with patient-reported outcomes and biological markers to better understand ICUAW after severe cardiorespiratory failure.
CONDITIONS
Recovery From ICUAW Following Severe Respiratory and Cardiac Failure
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to approximately 1 year
Participants recovering from severe cardiorespiratory failure supported by mechanical cardio-respiratory support are observed to assess muscle size, strength, physical function, and quality of life over time.
Multiple visits during admission and follow-up up to 1 year
Total: 1 location
1
St Bartholomew's hospital (Barts NHS trust)
London, United Kingdom, EC1A 7BE
Actively Recruiting
M
Mark Griffiths, PhD FRCP
A
Ashley Thomas, MSc
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Susannah A A Bloch, Anna V J Donaldson, Amy Lewis...
https://pubmed.ncbi.nlm.nih.gov/25888214