Investigation of Medial Longitudinal Arch and Foot Function in Patients With Lipedema

Recruiting Observational Study
Lipedema Hypermobility Syndrome (Disorder) Pes Planus Joint Hypermobility
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 65
Sex
Female
Study type
Observational
Participants needed
32 (estimated)
Sponsor
Marmara University · Other
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About This Trial
Lipedema is a chronic adipose tissue disorder that commonly leads to joint laxity, hypermobility, and functional limitations, yet its impact on foot morphology has not been systematically examined. This case-control study aims to investigate whether patients with lipedema exhibit a higher prevalence of generalized joint hypermobility and foot structural abnormalities-specifically pes planus-compar…
Trial Locations
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Eligibility Criteria
General Inclusion Criteria (Apply to All Participants) * Female participants * Age 18 years or older * Able to read and write (literacy requirement) * Availability of bilateral lateral foot radiographs obtained within the past 1 year in the hospital PACS system * Willing and able to provide written…
Contacts

Gökçenur Yalçın, M.D., PMR Specialist

+90 216 414 05 45

gokce_cihaner@hotmail.com

CONTACT