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Clinical Trials/NCT04328610
NCT04328610UnknownNot Applicable

A Randomized Controlled Trial to Assess the Efficacy of the Lymphatic Microsurgical Preventive Healing Approach (LYMPHA) to Prevent Lymphedema After Axillary Dissection for Breast Cancer

Pusan National University Hospital1 site in 1 country34 target enrollmentStarted: March 5, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
34
Locations
1
Primary Endpoint
limb volume

Study Overview

Brief Summary

Lymphedema is the Build-up of Lymph Fluid in the Body's Tissue Causing Chronic, Debilitating Swelling. This Commonly Occurs as a Result of a Disruption of the Lymphatic System During Lymph Node Dissection Surgeries. LYMPHA (LYmphatic Microsurgical Preventive Healing Approach) is an Innovative Microsurgical Technique Where Blocked Lymphatic Vessels Are Drained Into the Blood Circulation by Surgically Creating a Shunt Between a Lymphatic Channel and a Blood Vessel Called a Lymphatic-venous Bypass. Recently, LYMPHA Technique Has Been Shown to Prevent Lymphedema When Performed at the Time of Nodal Dissection. We Propose a Prospective Study Evaluating the Effectiveness of LYMPHA Technique Using Objective Clinical Protocol.

Detailed Description

Consenting patients will have the LYMPHA procedure at the time of planned axillary dissection surgery for the prevention of upper and extremity lymphedema. The node dissection will be performed by Dr. Kang while the LYMPHA technique will be performed by the plastic surgeon, Dr. Kim. The LYMPHA procedure consist of performing LVA at the time of the node dissection. Patent blue dye will be injected in the volar surface of the upper third of the arm in a quantity of about 1-2 ml intradermally, subcutaneously, and under muscular fascia into patient approximately 10 minutes before skin incision. This will allow mapping of the lymphatic channels for identification for bypass. The node dissection will then be performed with preservation of the anterior branch of the axillary vein in the axilla. Afferent lymphatic vessels will be sutured into a branch of the axillary vein distal to a competen valve. The total duration of the surgery is approximately 3 hours. The LYMPHA technique accounts for an additional 30 min to the standard 2-2.5 hours allocated to the node dissection.

Pre-surgery, patients will have baseline limb circumference measurements of both the surgery-affected and unaffected arms and by lymphoscintigraphy. Patients will be followed up clinically at every 6 months up to a year. At each follow-up visit, patients will have a physical examination and their circumference of their limbs taken. Patients will also fill out a LyQLI, SF-36, DASH administered by the Clinical Research Coordinator pre-and post-surgery. Each patient will have a total of 1 years of participation time.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Node-positive cancer requiring an axillary or lymphadenectomy
  • •Below 30 Body Mass Index

Exclusion Criteria

  • •Patients receiving a sentinel lymph node biopsy
  • •Patients with established preoperative lymphedema
  • •Patients with post-thrombotic syndrome, peripheral vascular disease
  • •Pregnant patients

Arms & Interventions

LYMPHA technique group

Experimental

LVA at the time of Axillary Dissection

Intervention: LYMPHA(LYmphatic Microsurgical Preventive Healing Approach) technique (Procedure)

Non-LYMPHA technique group

No Intervention

No preventive surgical approach

Outcomes

Primary Outcomes

limb volume

Time Frame: 1 year

Difference in limb volume between LYMPHA technique group and Non-LYMPHA technique group

lymphatic flow

Time Frame: 1 year

Difference in lymphatic flow between LYMPHA technique group and Non-LYMPHA technique group

lymphatic flow

Time Frame: 6 months

Difference in lymphatic flow between LYMPHA technique group and Non-LYMPHA technique group

limb volume

Time Frame: 6 months

Difference in limb volume between LYMPHA technique group and Non-LYMPHA technique group

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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