Clinical Trials Directory

Trials / Completed

CompletedNCT01096589

Assessment of 3M Oedema Reduction System in the Treatment of Lymphoedema Compared to Commercial Short-stretch Bandage

Preliminary Study to Assess the Effectiveness of 3M Oedema Reduction System in the Treatment of Lymphoedema Treatment Compared to Comprilan Short-stretch Bandage Compression Therapy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
82 (actual)
Sponsor
Solventum US LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Objectives. The primary objective of the study is to assess volume reduction in the treatment of lymphoedematous legs and arms with compression bandaging. Secondary objectives: * Assessment of safety * Quality of life * Health economic parameters * Slippage * Subbandage pressure

Conditions

Interventions

TypeNameDescription
DEVICE3M Coban 2 (Compression System)Nonwoven cohesive backing and foam.
DEVICE3M Coban 2 (Compression System)Nonwoven cohesive backing and foam.
DEVICE3M Coban 2 (Compression System)Nonwoven cohesive backing and foam.
DEVICEComprilanCommercial short-stretch bandage (Comprilan; BSN Medical Ltd, Hull, U.K).

Timeline

Start date
2010-03-01
Primary completion
2010-10-01
Completion
2010-10-01
First posted
2010-03-31
Last updated
2024-10-02
Results posted
2012-11-27

Locations

11 sites across 2 countries: United States, United Kingdom

Source: ClinicalTrials.gov record NCT01096589. Inclusion in this directory is not an endorsement.