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Clinical Trial Summary

A randomised prospective investigation of volume and quality of life results with lymphovenous anastomosis in patients with unilateral arm lymphedema after breast cancer using Indocyanine Green lymphangiography and MD Anderson Staging.


Clinical Trial Description

This is a randomized study comparing lymphovenous anastomosis versus conservative (compression) treatment for lymphoedema after breast cancer surgery - 50 patients to be included in each study arm. The primary endpoint is volume change measured by submersion and changes in arm circumference at defined levels from the wrist. Secondary endpoint is health related quality of life measured by questionnaire Short Form 36 (SF-36), Hospital Anxiety Depression Score (HADS), Fatigue Questionnaire (FQ) and a disease-specific questionnaire, Upper Limb Lymphedema score (ULL27). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03578380
Study type Interventional
Source Sykehuset Telemark
Contact Lars Johan Sandberg, MD
Phone +4735003456
Email johansandberg@hotmail.com
Status Recruiting
Phase N/A
Start date January 26, 2016
Completion date December 31, 2024

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