Skin glow may predict inflammation in FMF patients
NCT ID NCT07439341
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether a painless skin scan can measure long-term inflammation in people with Familial Mediterranean Fever (FMF). Researchers will compare these skin measurements with a blood-based inflammation score called the CALLY index. The goal is to better understand ongoing low-level inflammation even when patients feel well.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2026
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 patients diagnosed with Familial Mediterranean Fever and age- and sex-matched healthy volunteers recruited from a single tertiary care center.
- Ages
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18 to 65 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: For FMF Patients: * Age between 18 and 65 years * Diagnosis of Familial Mediterranean Fever according to Tel-Hashomer criteria * At least 6 months of clinical follow-up * Available routine laboratory data (CRP, albumin, lymphocyte count) * Not in an acute FMF attack at the time of assessment * Ability to provide written informed consent For Healthy Controls: * Age between 18 and 65 years * No history of chronic inflammatory, autoimmune, metabolic, or renal disease * Ability to provide written informed consent Exclusion Criteria : * Diagnosis of diabetes mellitus * Chronic kidney disease stage 3 or higher * Active infection * Malignancy within the past 5 years * Dermatologic condition affecting the forearm measurement site * Use of high-dose antioxidant or vitamin supplementation within the past 3 months * Any condition that, in the opinion of the investigators, may interfere with study participation
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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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