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Clinical Trial Summary

This randomized trial will test the effect of a prospective surveillance program for early detection and subclinical management of breast cancer-related lymphedema on the prevalence of chronic lymphedema.


Clinical Trial Description

Design and setting: This trial is a multi-center single-blind trial involving five hospitals in Denmark. Procedure: All women booked for surgery for breast cancer at one of the study sites will be invited to participate. Women, who provide written informed consent, will have BIS measurements, and perform self-measurements of arm circumference. Further, participants will complete a sociodemographic questionnaire which will be used to ensure recruitment of a representable sample. This data will be collected at the hospital of surgery at pre-treatment. After surgery, women who had >6 lymph nodes removed and have planned radiation therapy will be randomized 1:1 into intervention or control. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04522648
Study type Interventional
Source Rigshospitalet, Denmark
Contact Bolette S Rafn, PhD
Phone +45 22913873
Email bolette.skjoedt.rafn@regionh.dk
Status Recruiting
Phase N/A
Start date January 4, 2021
Completion date December 2026

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