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TerminatedNo phase

Preventing Lymphedema in Axillary Lymph Node Dissection

Reason given: slow accrual; diminished funding

Key facts

Where
Jacksonville and Rochester, United StatesSee the 2 sites

Where in United States

  • Mayo Clinic in FloridaJacksonville, United StatesNo longer taking part
  • Mayo Clinic in RochesterRochester, United StatesNo longer taking part

Trial details

Who runs it
Mayo Clinic
Trial code
NCT03428581
Record updated
24 February 2026
Original description
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.Read full original descriptionShow less

Preventing Lymphedema in Patients Undergoing Axillary Lymph Node Dissection Via Axillary Reverse Mapping and Lympho-venous Bypass

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.

Inclusion: Patients scheduled to undergo an axillary lymph node dissection; Patients who in the surgeon's judgement are at high risk to convert to an axillary lymph node dissection based intraoperative findings; English speaking.

Exclusion: Prior ipsilateral axillary lymph node dissection; Prior ipsilateral axillary radiation; Previous treatment for lymphedema of either arm or prescribed prophylactic treatment for lymphedema; Patients undergoing sentinel lymph node biopsy only or at low risk of converting to an axillary lymph node dissection in the surgeon's judgement; Pregnant patients cannot participate in the substudy.

ClinicalTrials.gov NCT03428581