Tick bite study aims to unlock secrets of sudden meat allergy
NCT ID NCT07177729
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at what happens in the body right after a tick bite. Researchers want to learn why some people develop a food allergy to red meat, called alpha-gal syndrome. About 100 adults who have been bitten by a tick will donate blood and their tick for testing. The goal is to find early signs that predict who will get the allergy.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Feb 2027
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
Adult population having experienced a recent tick bite and volunteering to visit the study clinic for blood donation at 2 time-points, respectively 3 time-points for a selected subgroup.
- 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: * Individuals aged ≥ 18 years, Male and Female. * Experience of a tick bite: the tick has been removed less than 48 hours ago, or the tick is still attached to the skin and can be removed on site by the study nurse. * Tick available for analysis. * Informed consent signed. Exclusion criteria: * Individuals \< 18 years of age, Male or Female. * Individuals with an acute viral/bacterial inflammation. * Individuals with an immune deficiency or under immunosuppressive treatments. * Individuals in receipt with immunotherapy with omalizumab. * Individuals with neurological diseases / impaired cognitive disorder.
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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 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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Centre Hospitalier du Luxembourg (CHL)
ACTIVE_NOT_RECRUITINGStrassen, Luxembourg
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LCTR
RECRUITINGLuxembourg, Luxembourg
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