Fish oil may unlock heart protection for dialysis patients
NCT ID NCT07730385
First seen Jul 28, 2026 · Last updated Aug 05, 2026 · Updated 3 times
Summary
People on maintenance hemodialysis face a high risk of heart disease, and standard cholesterol drugs often fail to help. This trial tests whether high-dose fish oil (4 grams daily for 8 weeks) can improve the function of HDL, the 'good' cholesterol, which may become faulty in kidney failure. Forty adults on dialysis will take part in a crossover study, with each person receiving fish oil and a period without it. The main goal is to measure how well HDL removes cholesterol from cells, which could explain a recent finding that omega-3s reduce heart events in this group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- fish oil (omega-3 fatty acids)
- What this could lead to
- If omega-3s improve HDL function, this could point toward a way to lower heart disease risk in people on dialysis.
- What could go wrong
- This is a small, early mechanistic study, not designed to prove clinical benefit. The results may not lead to changes in treatment.
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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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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 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.
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 * receiving maintenance in-center hemodialysis * able to provide written informed consent * clinically stable condition (no hospitalization within 4 weeks prior to baseline) Exclusion Criteria: * inability or unwillingness to provide informed consent * known hypersensitivity or intolerance to fish oil or n-3 PUFA-containing products * use of n-3 PUFA supplements at baseline or within the preceding 8 weeks * pregnancy * acute infection, hospitalization or major inflammatory condition at the time of baseline assessment * any condition that, in the investigator's opinion, would make participation unsafe or interfere with study participation or data interpretation * inherited lipid metabolism disorders
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names. We don't republish those.
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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.
Contacts and locations
Locations
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Chronic Hemodialysis Unit, Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna
Vienna, State of Vienna, 1090, Austria
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