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Can running 100km change your Eye's blood vessels?
NCT ID NCT07748936
First seen Aug 06, 2026 · Last updated Aug 07, 2026 · Updated 1 time
Summary
This pilot study looks at whether running an ultra-trail race—a very long, intense endurance event—causes temporary changes in the tiny blood vessels at the back of the eye. Researchers will use a non-invasive imaging technique called OCT angiography to measure blood flow in the retina and choroid of ultra-trail runners before and shortly after the race. They will compare these measurements to a control group of active people who do not run the race. The goal is to understand how extreme physical exertion affects eye circulation and whether retinal imaging could serve as a window into overall cardiovascular health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Retinal imaging (OCT angiography and retinophotography) before and after an ultra-trail race
- What this could lead to
- If this works, it could show that simple eye scans can reveal how extreme exercise stresses the body's blood vessels, potentially aiding cardiovascular research and prevention.
- What could go wrong
- This is a small pilot study, so results may not apply broadly. Changes in eye blood flow after a race might be temporary and not reflect long-term health.
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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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: * Participant who has given free, informed, and verbal consent * Participant of legal age * Participant registered for the UTMA 100 km solo ultra-trail race (for the "ultra-trail" group) * Active subject not exposed to intense physical exertion (\>6 hours of exercise) within the 7 days prior to the enrollment visit (for the "active control" group) * Participant with an estimated physical activity level of 4-6 hours per week (for the "active control" group) * Participant agreeing to undergo ophthalmological examinations on the same schedule as the ultra-trail group (for the "active control" group) Exclusion Criteria: * Myopia \> 6 diopters * Type 1 or Type 2 diabetes * Protected individuals: Minors, individuals under legal protection (guardianship, conservatorship, court order), individuals unable to give informed consent * Individuals not enrolled in a social security program * Pregnant or breastfeeding women * Participants with a systemic or inflammatory vascular condition and cardiovascular risk * Participants with an ocular condition or ophthalmological history likely to impair retinal/choroidal microcirculation or the quality of imaging (vascular and degenerative macular conditions, cataracts) * Participants being treated with vasoconstrictors * Tobacco use within 4 hours prior to enrollment * Caffeine consumption within 1 hour prior to enrollment
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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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Chu Dijon Bourgogne
Dijon, 21000, France
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