Fish oil supplement aims to help head and neck cancer patients through tough treatment
NCT ID NCT07180576
First seen Jun 26, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This pilot study will test whether a fish oil-enriched nutritional supplement, combined with weekly nutrition counseling, is feasible and safe for people with head and neck cancer undergoing chemoradiotherapy. Fifteen participants will start taking the supplement two weeks before treatment and continue through the end of radiation. The study will measure how many people can stick with the supplement, any side effects, and whether it helps maintain body weight and nutrition.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Fresubin Supportan (fish oil-enriched high calorie, high protein oral nutrition supplement) and weekly nutrition counseling
- What this could lead to
- If successful, this could show that adding a fish oil supplement and nutrition counseling helps patients with head and neck cancer better tolerate chemoradiotherapy and maintain their nutrition.
- What could go wrong
- This is a very small pilot study (15 people) focused on feasibility, not on proving the supplement works. It is too early to know if it will improve outcomes, and some patients may have side effects from the supplement.
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.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
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.
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: * Newly diagnosed with Stage I - IV oral cavity, hypopharyngeal, oropharyngeal, or laryngeal cancer * Age 18+ * Planned for definitive radiotherapy with or without surgery and chemotherapy Exclusion Criteria: * Metastatic disease * Prior head/neck RT * Presence of malnutrition at diagnosis per ASPEN criteria * Prior cancer within 3 years (except non-melanoma skin cancer and cervical carcinoma in situ) * Inability to consent * Severe psychiatric illness * Medical conditions impairing participation/adherence * Non-adults, pregnant women, prisoners, and other legally protected vulnerable groups * Dairy, soy, and/or fish allergy * Non-English speaking * Documented history of atrial fibrillation or other significant arrhythmias * Receiving therapeutic anticoagulation (e.g., warfarin, direct oral anticoagulants) and/or clotting disorders (e.g., hemophilia, thrombocytopenia)
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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
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The official record
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