Actively Recruiting

Phase Not Applicable
Age: 20Years - 80Years
All Genders
Healthy Volunteers
NCT06041958

Effects of Extracorporeal Shock Wave Therapy and Pulse Electromagnetic Field Therapy on Lymphoedema

Led by Zheng-Yu Hoe, MD., PhD. · Updated on 2026-03-31

90

Participants Needed

1

Research Sites

272 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Lymphedema occurs not only in patients with breast cancer and gynecological cancers but also in those where lymphatic drainage is obstructed. Accumulation of lymphatic fluid within tissues results in limb swelling. Additionally, proteins present in lymphatic fluid might lead to fibrosis within tissues, causing various challenges for patients. The changes in volume and weight can significantly impact daily life activities such as eating, brushing teeth, and other routine tasks. Furthermore, it can lead to clothing difficulties and provoke unwanted attention due to aesthetic concerns. Currently, there is no definitive treatment for lymphedema. However, prospective research has shown promising results in applying extracorporeal shock wave therapy (ESWT), originally used for musculoskeletal disorders like plantar fasciitis, tennis elbow, frozen shoulder, and non-union fractures, to lymphedema patients. Similarly, Pulse Electromagnetic Field Therapy (PEMFT), widely used for pain management and muscle strengthening, has the potential for treating lymphedema as it can enhance blood circulation and stimulate muscle contractions. This research project aims to explore the effectiveness and sustainability of using ESWT and PEMFT for lymphedema patients. By applying these therapies to lymphedema patients, this study aims to evaluate their treatment outcomes and long-term effects.

CONDITIONS

Official Title

Effects of Extracorporeal Shock Wave Therapy and Pulse Electromagnetic Field Therapy on Lymphoedema

Who Can Participate

Age: 20Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be at least 20 years old and able to understand instructions, communicate, and sign informed consent
  • Diagnosis of lymphedema after breast cancer or gynecologic cancer treatment with limb circumference difference greater than 2 cm
  • Ability to attend follow-up appointments during the 12-month study period, referred by a rehabilitation physician
Not Eligible

You will not qualify if you...

  • Presence of unhealed open wounds, acute infections, or other conditions unsuitable for contact treatment on the affected limb
  • Affected limb has metastatic tumors
  • Affected limb has untreated deep vein thrombosis
  • Severe clotting abnormalities

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

Kaohsiung Veterans General Hospital

Kaohsiung City, Taiwan, 81362

Actively Recruiting

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Research Team

Z

Zheng Yu Hoe, MD.,PhD.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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