Fact CheckerSign in

NCT07520942Completed

TECAR and ESWT in Obesity-Related Lower Limb Lymphedema

The Effect of TECAR Therapy and Extracorporeal Shock Wave Therapy Combined With Complex Decongestive Therapy in the Treatment of Bilateral Lower-Limb Secondary Lymphedema in Severely Obese Patients: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 9 Apr 2026

Brief summary (registry, in English)

This randomized controlled trial evaluates the effectiveness of adding TECAR therapy or extracorporeal shock wave therapy (ESWT) to complex decongestive therapy (CDT) in the treatment of bilateral lower-limb lymphedema in severely obese patients. Forty-five female participants were randomly assigned to one of three groups: CDT alone, CDT combined with TECAR, or CDT combined with ESWT. The interventions were applied over a four-week period. The primary outcome was reduction in limb circumference, while secondary outcomes included quality of life, pain intensity, and tissue stiffness. Assessments were conducted at baseline, after 4 weeks of treatment, and at 8 weeks follow-up.

Status (registry)
Completed
Study type
Interventional
Enrollment
45 (actual)
First submitted
3 Apr 2026
Start date
25 Oct 2025
Primary completion date
6 Feb 2026
Lead sponsor
Applied Science Private University
Diseases
Obesity
NCT number
NCT07520942

What you commit to

  • Study type: Interventional
  • Participants enrolled: 45
  • From 25 Oct 2025 to the primary completion date, 6 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindications to ESWT or TECAR therapy including pacemaker or implanted electronic devices
  • Patients receiving concurrent lymphedema treatment or those who had received intensive treatment within the preceding 3 months

Other illness

  • Secondary lymphedema due to malignancy, radiation, surgery, or infection
  • Acute deep vein thrombosis or history of recurrent thrombosis
  • Active infection or cellulitis
  • Peripheral arterial disease with ankle-brachial index below 0.8
  • Uncontrolled cardiac failure or renal insufficiency

Other

  • Primary lymphedema
  • Pregnancy or lactation

Who the study is looking for

  • Female patients aged 18-75 years with bilateral lower limb lymphedema secondary to severe obesity (BMI ≥40 kg/m²)
  • Lymphedema duration of at least 3 months
  • Clinical diagnosis confirmed by an experienced lymphedema specialist with bilateral limb swelling (pitting or non-pitting edema extending above the ankle)
  • Ability to attend treatment sessions five times weekly for 4 weeks and follow-up assessments

Age in the registry: 18 years to 75 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Modawah Physical Therapy Center
Coordinator of this site? Confirm its status
Banī SuwayfEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.