Clinical trial Recruiting at 1 site Observational Ages 18 and up

Understanding muscle wasting in cancer patients

Official title: Routine Evaluation of People Living With Cancer - Surgery

Run by University of Edinburgh · NCT05642819 · Data updated 2026-11-12

This study looks at cancer patients who are losing muscle and weight to see how their body, activity levels, and overall well-being change over time.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment200 (estimated)
SponsorUniversity of Edinburgh
Academic / other
Locations1 site (Edinburgh)
StatusRecruiting
StartedOctober 1, 2023
Main results expectedDecember 2027
Study endsDecember 2027
Registry record updatedDecember 2, 2025
Trial IDNCT05642819 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and over with cancer who are scheduled for surgical resection of malignancies in the oesophagus, stomach, pancreas, colon, or rectum.

Probably not a fit

Patients with concomitant inflammatory or muscle wasting conditions other than cancer, or those with significant medical or psychiatric issues, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on patients with cancer who are at risk of cachexia, a condition characterized by muscle wasting and weight loss. It aims to gather comprehensive data on body composition, physical activity, quality of life, and immune response to cancer over time. By examining these factors together rather than in isolation, the study seeks to provide a more complete understanding of how cachexia affects surgical patients. The findings could help improve patient management and outcomes in those undergoing cancer treatment.

Why it matters

Potential benefit: If successful, this study could lead to better strategies for managing cachexia in cancer patients, potentially improving their quality of life and treatment outcomes.

How similar studies have gone: While cachexia has been studied in various contexts, this holistic approach to understanding its impact on surgical patients is relatively novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Inclusion Criteria (Cancer Resection)

* Patients with cancer (Clinical, histological, cytological or radiological evidence) planned for surgical resection of a malignancy of the oesophagus, stomach, pancreas, colon, or rectum
* Aged 18-years and over
* Able to give written informed consent

Inclusion Criteria (Healthy Controls)

* Patients identified at surgical clinic as being planned for an open abdominal operation for a non-inflammatory, benign condition (e.g. donor nephrectomy)
* Aged 18-years and over
* Able to give written informed consent

Exclusion Criteria:

* Any concomitant medical or psychiatric problems which, in the opinion of the investigator, would increase the risk of complication for the participant and/or investigator
* Presence of a concomitant inflammatory (e.g., rheumatoid arthritis, inflammatory bowel disease) or muscle wasting condition other than cancer
* Participants who are pregnant, suffer from claustrophobia or with implanted medical devices (e.g., cardiac pacemaker, metallic foreign bodies, aneurysm clip) would not be able to undergo the additional multiparametric magnetic resonance imaging (MRI)

Where it's running

  • University of Edinburgh
    Edinburgh, United Kingdom
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.