Preventing Lymphedema in Axillary Lymph Node Dissection

Status Active, not recruiting

Clinical Trial Summary

The researchers are trying to answer if axillary reverse mapping (ARM) with lympho-venous bypass (LVB) in patients undergoing an axillary lymph node dissection reduces the rate and severity of post-operative lymphedema of the arm.

Clinical Trial Description

All subjects will undergo an axillary lymph node dissection (ALND). Cluster randomization will determine which of these subjects will have the ARM with LVB and which subjects will have the ALND without this technique. As a baseline, all subjects will have the circumference of their arms measured and complete a questionnaire about lymphedema. Performing the measurements and answering a questionnaire will be repeated at 6, 12, 24, and 36 months after surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03428581
Study type	Interventional
Source	Mayo Clinic
Contact
Status	Active, not recruiting
Phase	N/A
Start date	April 10, 2018
Completion date	February 28, 2026

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