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To Assess the Efficacy of the LYMPHA in the Prevention of Lymphedema Following Axillary Dissection for Breast Cancer (LYMPHA)

Primary Purpose

Lymphedema, Breast Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
LYMPHA(LYmphatic Microsurgical Preventive Healing Approach) technique
Sponsored by
Pusan National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphedema, Breast Cancer

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Pusan National University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

LYMPHA technique group

Non-LYMPHA technique group

Arm Description

LVA at the time of Axillary Dissection

No preventive surgical approach

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Full Information

First Posted
March 29, 2020
Last Updated
March 13, 2021
Sponsor
Pusan National University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04328610
Brief Title
To Assess the Efficacy of the LYMPHA in the Prevention of Lymphedema Following Axillary Dissection for Breast Cancer
Acronym
LYMPHA
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 5, 2020 (Actual)
Primary Completion Date
February 28, 2022 (Anticipated)
Study Completion Date
February 28, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pusan National University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphedema, Breast Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
34 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LYMPHA technique group
Arm Type
Experimental
Arm Description
LVA at the time of Axillary Dissection
Arm Title
Non-LYMPHA technique group
Arm Type
No Intervention
Arm Description
No preventive surgical approach
Intervention Type
Procedure
Intervention Name(s)
LYMPHA(LYmphatic Microsurgical Preventive Healing Approach) technique
Intervention Description
Patients will receive a lymphatic-venous anastomosis at time of their required Axillary Dissection
Primary Outcome Measure Information:
Title
lymphatic flow
Description
Difference in lymphatic flow between LYMPHA technique group and Non-LYMPHA technique group
Time Frame
6 months
Title
limb volume
Description
Difference in limb volume between LYMPHA technique group and Non-LYMPHA technique group
Time Frame
6 months
Title
lymphatic flow
Description
Difference in lymphatic flow between LYMPHA technique group and Non-LYMPHA technique group
Time Frame
1 year
Title
limb volume
Description
Difference in limb volume between LYMPHA technique group and Non-LYMPHA technique group
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jin A Yoon, MD, Ph.D
Phone
+82-51-240-7845
Email
yjk5289@naver.com
Facility Information:
Facility Name
Pusan National University Hospital
City
Busan
State/Province
Seo-Gu
ZIP/Postal Code
49241
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jin A Yoon, MD, Ph.D
Phone
+82-51-240-7485
Email
yjk5289@naver.com

12. IPD Sharing Statement

Learn more about this trial

To Assess the Efficacy of the LYMPHA in the Prevention of Lymphedema Following Axillary Dissection for Breast Cancer

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