TECAR and ESWT in Obesity-Related Lower Limb Lymphedema

Applied Science Private University

Status: Completed

Conditions: Obesity & Overweight; Lymphedema

Treatments: Device: TECAR Therapy; Other: Complex Decongestive Therapy; Device: Extracorporeal Shock Wave Therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT07520942

SREC.PT.SUE (19)1025

Details and patient eligibility

About

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.

Full description

Lymphedema associated with severe obesity is a chronic and progressive condition characterized by bilateral lower-limb swelling, pain, reduced mobility, and impaired quality of life. Complex decongestive therapy (CDT) is considered the standard treatment; however, its effectiveness may be limited in patients with severe obesity due to underlying fibrosis, inflammation, and adipose tissue accumulation.

Adjunctive therapies such as transfer energy capacitive and resistive (TECAR) therapy and extracorporeal shock wave therapy (ESWT) have been proposed to enhance treatment outcomes. TECAR therapy uses radiofrequency energy to improve microcirculation and promote lymphatic drainage, while ESWT may stimulate lymphangiogenesis and reduce tissue fibrosis.

This prospective randomized controlled trial aimed to compare the effectiveness of CDT alone with CDT combined with TECAR or ESWT in severely obese patients with bilateral lower-limb lymphedema. A total of 45 female participants were randomly assigned into three groups: CDT alone, CDT plus TECAR therapy, and CDT plus ESWT. All interventions were administered over a four-week period.

Outcome measures included limb circumference as the primary outcome, and quality of life (LYMQOL), pain intensity (VAS), and tissue stiffness (tonometry) as secondary outcomes. Assessments were conducted at baseline, after 4 weeks of treatment, and at 8 weeks follow-up.

The findings of this study aim to provide evidence on the effectiveness of adjunctive therapies in improving clinical outcomes in obesity-related lymphedema and support clinical decision-making in this population.

Enrollment: 45 patients

Sex: Female

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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

Exclusion criteria

• Secondary lymphedema due to malignancy, radiation, surgery, or infection
• Primary lymphedema
• 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
• Pregnancy or lactation
• 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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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45 participants in 3 patient groups

CDT

Experimental group

Description:

Participants receive complex decongestive therapy including manual lymphatic drainage, compression bandaging, therapeutic exercises, and skin care.

Treatment:

Other: Complex Decongestive Therapy

CDT + TECAR

Experimental group

Description:

Participants receive complex decongestive therapy combined with TECAR therapy, a radiofrequency treatment applied to improve microcirculation and lymphatic drainage.

Treatment:

Other: Complex Decongestive Therapy

Device: TECAR Therapy

CDT + ESWT

Experimental group

Description:

Participants receive complex decongestive therapy combined with extracorporeal shock wave therapy applied to enhance lymphatic function and reduce tissue fibrosis.

Treatment:

Device: Extracorporeal Shock Wave Therapy

Other: Complex Decongestive Therapy