Omega-3 drink may fight cancer malnutrition
NCT ID NCT07255066
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a special omega-3-enriched nutritional drink can improve nutrition in people with advanced lung or colorectal cancer who are at risk of malnutrition. About 118 participants will either get the drink plus dietary advice, or just dietary advice alone. The goal is to see if the drink helps with weight, muscle strength, inflammation, and quality of life.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 118 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
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.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participants with stage III-IV lung and/or colorectal cancer undergoing systemic anti-cancer treatment (SACT) or starting SACT within the next 4 weeks \*with non-curative intent * Participants aged 18 or older * Participants at nutritional risk defined as a BMI \<20 kg/m2 and/or weight loss between 5-10% in the previous 6 months\*\* * Participants with systemic inflammation within 28 days of screening (e.g. CRP \>10 mg/dL) * Participants with an ECOG-PS\*\*\* score of 0, 1 or 2 * Participants willing and able to give written informed consent Exclusion Criteria: * Participants with a recent history of tumour resection (within 12 months) * Participants who have lost \>10% body weight in the previous 6 months before baseline - observed or participant reported. * Participants with severe renal or hepatic failure or an intolerance to any of the ingredients of the study product * Participants who are using dietary counselling, ONS or any form of artificial feeding at the time of recruitment * Unable to adhere to either arm of the trial and appropriate requirements * Contraindication to ONS including a lactose intolerance * Females who are pregnant or of childbearing potential and not using adequate contraception
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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