Lymphovenous Bypass Procedure for Secondary Prevention of Lymphedema in Breast Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDharmais National Cancer Center Hospital

About this trial

This study aims to evaluate the effectiveness of the Lymphovenous Bypass (LVB) procedure compared to physiotherapy alone as secondary prevention of lymphedema in breast cancer patients undergoing axillary lymph node dissection.

Eligibility criteria

Qualifiers

Breast cancer patients aged ≥ 18 years with an ECOG score > 1

Breast cancer patients with post-axillary lymph node dissection diagnosed with stage 0 and I lymphedema.

Those who have never undergone lymphedema physiotherapy.

Disqualifiers

Patients with dermal backflow before axillary lymph node dissection (ALND).

Patients with breast cancer lymphedema who are unable to undergo a 24-month follow-up at Dharmais Cancer Hospital.

Patients with iodine allergy, severe asthma, decreased kidney function, pregnancy, or breastfeeding.

Trial design

Treatments tested in this trial

  • Lymphovenous bypass (LVB)

Treatment groups

136 Participants
are divided into 2 treatment groups