The Relationship Between Central Sensitization, Pain, and Psychosocial Factors in Individuals With Lipedema
NCT ID: NCT07240285
Last Updated: 2025-11-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
60 participants
OBSERVATIONAL
2025-10-10
2025-11-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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Lipedema group
Patients with lipedema
No interventions assigned to this group
Control group
Patients without lipedema
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Aged between 18 and 75 years
* Provided voluntary informed consent
Exclusion Criteria
* Presence of neurological disorders (e.g., polyneuropathy, multiple sclerosis, history of stroke)
* Currently under active psychiatric treatment Pregnancy
* History of lower extremity surgery or major trauma within the past 6 months
* Received injection therapy or physical therapy for the lower extremities within the past 6 -months
* History of infection or active dermatological disease affecting the lower extremities
18 Years
75 Years
FEMALE
No
Sponsors
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Istanbul Physical Medicine Rehabilitation Training and Research Hospital
OTHER_GOV
Responsible Party
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Locations
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Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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Istftreah
Identifier Type: -
Identifier Source: org_study_id
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