A diet tweak may boost platelets in a bleeding disorder
NCT ID NCT07798050
First seen Sep 01, 2026 · Last updated Sep 04, 2026 · Updated 3 times
Summary
This trial tests whether adding a selective Mediterranean diet to standard treatment can improve platelet counts and reduce bleeding in adults with immune thrombocytopenia (ITP), a condition where the immune system attacks platelets. Sixty adults aged 18 to 60 with low platelet counts will be randomly assigned to either the diet plus standard therapy or standard therapy alone. Over 12 weeks, researchers will measure changes in platelet counts and bleeding severity to see if the diet offers extra benefit.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A selective Mediterranean diet regimen, used alongside standard ITP medications such as corticosteroids or intravenous immunoglobulin
- What this could lead to
- If it works, this diet could become a simple, safe addition to standard ITP treatment, helping patients raise their platelet counts and reduce bleeding without extra drugs.
- What could go wrong
- This is a small, early-stage trial, so the diet may not meaningfully improve platelet counts or bleeding. Dietary changes can be hard to follow, and results may not apply to all ITP patients.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 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 to 60 years
- 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 18-60 years * Diagnosis of primary immune thrombocytopenia according to American Society of Hematology (ASH) criteria * Platelet count \< 100 × 10⁹/L at enrollment * Willingness to comply with the dietary protocol and follow-up schedule Exclusion Criteria: * Secondary thrombocytopenia * Pregnancy or lactation * Uncontrolled diabetes mellitus, chronic kidney disease, or hepatic failure * Strict dietary regimens for other medical conditions * History of bariatric surgery or malabsorption syndromes * Known food allergies to core Mediterranean diet components * Active chemotherapy or splenectomy within the last 3 months * Prednisone/prednisolone ≥ 20 mg/day (or equivalent) at enrollment or recent dose adjustment within 2 weeks * Poor compliance or inability to attend follow-up visits
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. 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.
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Other studies related to the condition(s) this trial covers.
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