Actively Recruiting

Age: 18Years - 75Years
FEMALE
Healthy Volunteers
NCT07489248

Multimodal Ultrasound for Differentiating Lymphedema and Lipedema

Led by Kayseri City Hospital · Updated on 2026-03-24

75

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this observational study is to evaluate the diagnostic value of multimodal ultrasonography in differentiating between lymphedema and lipedema. Differentiating these two chronic conditions based solely on clinical examination can be challenging due to overlapping symptoms. This study will utilize various non-invasive ultrasound techniques-including B-mode ultrasound, strain elastography, power Doppler, and quantitative ImageJ analysis-to compare tissue characteristics among patients with lymphedema, patients with lipedema, and healthy controls. The goal is to identify reliable, non-invasive imaging biomarkers that can facilitate early and accurate diagnosis, thereby optimizing patient management.

CONDITIONS

Official Title

Multimodal Ultrasound for Differentiating Lymphedema and Lipedema

Who Can Participate

Age: 18Years - 75Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 18 to 75 years
  • Clinical diagnosis of lower extremity lymphedema (for the lymphedema group)
  • Clinical diagnosis of lower extremity lipedema (for the lipedema group)
  • Healthy individuals with no history or clinical signs of chronic lower extremity edema (for the control group)
Not Eligible

You will not qualify if you...

  • Presence of active local infections, such as cellulitis or erysipelas, in the lower extremities
  • History of deep vein thrombosis (DVT) or severe chronic venous insufficiency
  • Systemic conditions causing secondary edema, including congestive heart failure, chronic kidney disease, or severe hepatic impairment
  • Previous surgical interventions on the affected lower extremities, including liposuction, lymphatic reconstructive surgery, or major orthopedic surgeries
  • Active malignancy or currently undergoing radiotherapy/chemotherapy
  • Pregnancy or lactation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kayseri City Hospital

Kayseri, Kocasinan, Turkey (Türkiye), 38080

Actively Recruiting

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Research Team

A

Abdullah Goktug Yazar

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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