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NOT YET RECRUITING
NCT07240415
NA

ESWT for Primary Lipedema

Sponsor: Fatih Bagcier

View on ClinicalTrials.gov

Summary

This randomized controlled clinical trial aims to evaluate the effectiveness of extracorporeal shockwave therapy (ESWT) when added to standard conservative treatment in women with primary lipedema. Participants will be randomly assigned to receive either standard conservative therapy alone or standard therapy combined with radial ESWT. The study will assess changes in pain intensity (VAS), limb circumference measurements, quality of life (SF-36), and patient satisfaction over an 8-week period. Evaluations will be performed at baseline, at the end of the 4-week treatment phase, and at 4-week follow-up. This trial seeks to provide evidence on whether ESWT offers additional clinical benefit in the management of primary lipedema.

Official title: Extracorporeal Shockwave Therapy for Primary Lipedema: A Randomized Controlled Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2025-12-01

Completion Date

2026-08-01

Last Updated

2025-11-20

Healthy Volunteers

No

Conditions

Interventions

OTHER

Standard Conservative Therapy

Manual lymphatic drainage, pneumatic compression, Class II compression garments, and a home-based exercise program.

DEVICE

radial ESWT

adial extracorporeal shockwave therapy using a BTL device (2.0-2.5 bar, 12 Hz, 1000 shocks per region, 20-mm head), twice weekly for 4 weeks (8 sessions).