New study aims to catch hidden malnutrition in chemo patients
NCT ID NCT07163286
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looks at 200 adults with solid tumors who are getting chemotherapy. Researchers will compare four different checklists (PG-SGA, MUST, Nutriscore, and GLIM criteria) to see which best identifies malnutrition and muscle loss. The goal is to find the most reliable tool so doctors can offer nutritional help sooner. No new drugs or treatments are being tested.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better identify cancer patients at risk of malnutrition and muscle loss, leading to earlier nutritional support.
- What could go wrong
- This is an observational study, not a treatment trial. It will not directly improve patient outcomes, and results may not apply to all cancer types or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Apr 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study will include approximately 150 adult outpatients (≥18 years) diagnosed with solid tumors (e.g., breast, lung, gastrointestinal, gynecologic cancers) who are currently receiving chemotherapy. Participants must have undergone or be scheduled for an abdominal CT scan within the last 3 months and must be physically and mentally capable of completing the assessments. Hospitalized patients and those with hematologic malignancies will be excluded.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years * Diagnosed with a solid tumor (e.g., breast, lung, GI, gynecologic cancers) * Receiving active outpatient chemotherapy * Recent abdominal CT scan within the last 3 months or planned * Provided written informed consent * Physically and mentally able to complete study procedures Exclusion Criteria: * Declined or unable to give informed consent * Cognitive impairment or mental status preventing participation * Neuromuscular diseases affecting muscle mass (e.g., myopathy, MND, severe neuropathy) * Inadequate CT image quality for L3 analysis * Acute infection or illness within the past month * Upper limb deformity or severe pain preventing handgrip testing * Incomplete assessments or withdrawal of consent during the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Çanakkale Onsekiz Mart University
Çanakkale, 17020, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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