Clinical Trials Directory

Trials / Unknown

UnknownNCT01954654

Effectiveness of Accelerated Intervention With Compression Sleeve in Mild and Moderate Breast Cancer-related Lymphedema

Effectiveness of Accelerated Intervention With Custom-made Compression Sleeve in Women With Mild and Moderate Arm Lymphedema Secondary to Breast Cancer Treatment

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
84 (estimated)
Sponsor
Mette Brodersen Jerver · Academic / Other
Sex
Female
Age
18 Years – 95 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether accelerated treatment with custom-made compression sleeve is more effective than standard procedure in the treatment of mild and moderate arm lymphedema secondary to primary cancer treatment.

Detailed description

Use of a custom-made compression sleeve is an initial treatment of mild and moderate arm lymphedema secondary to primary breast cancer treatment. The compression sleeve improves the flow of lymph fluid out of the arm, reduces the swelling, and prevents progression of the lymphedema in the future. Early intervention is recommended though early is not well-defined in literature. The purpose of this study is to evaluate reduction of excess limb volume and changes in arm disability and clinical symptoms in accelerated treatment with compression sleeve compared to standard treatment.

Conditions

Interventions

TypeNameDescription
DEVICECustom-made compression sleeve and -gauntletDevice: Compression garments worn for a minimum of six hours per day
OTHEREducational information, recommendation and instructionEducational information and recommendations about lymphedema and skin care. Instruction in physical exercises to enhance the lymph flow

Timeline

Start date
2013-10-01
Primary completion
2015-04-01
First posted
2013-10-07
Last updated
2013-10-08

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01954654. Inclusion in this directory is not an endorsement.