Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07233863

Lymphovenous Bypass Procedure for Secondary Prevention of Lymphedema in Breast Cancer

Effectiveness of Lymphovenous Bypass Procedure for Secondary Prevention of Lymphedema in Breast Cancer

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
136 (estimated)
Sponsor
Dharmais National Cancer Center Hospital · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

In the intervention group, LVB was performed with intima-to-intima coaptation using the super microsurgery technique. The anastomosis was between the afferent lymphatic vessel and the recipient vein. The upper extremity lymphedema (UEL) index and indocyanine green (ICG) lymphography are utilized to evaluate the progression of lymphedema.

Conditions

Interventions

TypeNameDescription
PROCEDURELymphovenous bypass (LVB)The Lymphovenous Bypass (LVB) procedure in this study is a microsurgical supermicrosurgery-based intervention specifically designed for the secondary prevention of breast cancer-related lymphedema following axillary lymph node dissection.

Timeline

Start date
2024-03-18
Primary completion
2027-03-21
Completion
2028-03-21
First posted
2025-11-18
Last updated
2025-11-18

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT07233863. Inclusion in this directory is not an endorsement.