Does your diet affect the blood you donate? new study investigates
NCT ID NCT07558369
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This observational study will enroll over 1,000 blood donors to see if their lifestyle and nutrition affect the quality of stored red blood cells. Researchers will measure damage that happens during storage and track how transfusions affect newborns and postpartum women. The goal is to learn how donor habits might impact patient safety.
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 1,014 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2029
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 population consists of candidates for whole blood donation at the Blood Bank (BDS) of the National Institute of Perinatology (INPer). All candidates must first complete standard Blood Bank procedures, including medical interview, complete blood count screening, blood collection, and infectious disease testing, in accordance with institutional protocols. Candidates deemed eligible for donation following routine evaluation will be invited to participate in the study. Those who agree will provide study-specific informed consent. Participation involves additional assessments beyond standard Blood Bank procedures.
- Ages
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18 to 64 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Eligible candidates according to Mexican regulatory standards for blood donation (NOM-253-SSA1-2012) Exclusion Criteria: \- Refusal to provide specific informed consent for participation in the research
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Genom att skicka in godkänner du våra Användarvillkor
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 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.
Contacts and locations
Locations
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Instituto Nacional de Perinatología
Mexico City, Mexico City, 11000, Mexico
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