MedPath

Comparison of Two Types of Bandages in the Treatment of Lymphoedema

Completed
Conditions
Lymphoedema
Registration Number
NCT05169086
Lead Sponsor
University Hospital, Montpellier
Brief Summary

The study is a cohort study of patients at the University Hospital during the first two days of intensive treatment. The patients are randomly divided into two groups (N=10).

Throughout the study, group A is treated with the multilayer elastic bandage while group B is bandaged with contention only. The bandages were applied on the first and second day and were maintained in place. The bandages were applied on the first and second day and were maintained for 24 hours. All patients performed 30 minutes of physical activity in the bandage on both days.

The evaluation is based on the volumetric difference, skin quality and quality of life of these patients

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Perimetry of the affected limbDay 2

The physiotherapist measures the perimeter of the limb with a tape measure

Volumetry of the affected limbDay 2

the volume is calculated using computer software.

Secondary Outcome Measures
NameTimeMethod
Quality of life questionnaireone month later

The patient completes the Lymphoedema Quality of Life Questionnaire (LYMQUOL leg) on admission to the ward and by email one month later

Trial Locations

Locations (1)

Uhmontpellier

🇫🇷

Montpellier, France

© Copyright 2025. All Rights Reserved by MedPath