Lymphedema Clinical Trial
Official title:
Prospective, Randomized Controlled Trial Comparing the Effect of CircAid(R) Juxta-Fit(tm) Versus Trico Bandages in the Treatment of Leg Lymphedema
Juxta-Fit is used for compression treatment. Juxta-Fit is an inelastic compression device which can be easily adjusted to the circumference of the limb and is usually used during the maintenance phase of lymphedema treatment. The aim of the study is to assess the effectiveness of Juxta-Fit in the initial treatment phase of leg lymphedema compared to the traditional treatment with Trico bandages in relation to interface pressure and to explore if self-management by Juxta fit is efficient after a short demonstration. Data are collected at 0-2-24 hours
Application of marketed compression systems (Juxta-Fit or Trico bandages) used for treatment
by trained specialists with assessment of the interface pressure and volume reduction. For
the first two hours, bandages and Juxta fit will be applied by experienced medical staff and
the use of the juxta-fit device will be explained to the patient. Thereafter the devices
will be removed and patients in the Juxta fit group will apply the device themselves in the
treatment. In this second phase after 2 hours, patients may adjust the Juxta-Fit according
to their needs and comfort when they feel the device is getting too loose as activity of
self-management during 24 hours. The patient will document this in a diary.
Detailed measuring data:
Volumetry:
Measurements after 0h, 2h and 24 h by using classic water displacement apparatus.
Pressure:
Measurements after 0h, 2h (pre and post system change) and 24 h at the B1 region:
- Supine and standing to calculate the Static Stiffness Index (SSI);
- Supine with and without dorsal flexion to calculate the Dynamic Stiffness index (DSI).
Circumference measurement as safety parameter At 5 cm above the upper part of the patella
the circumference is measured at 0-2-24 hours to monitor eventual fluids shift.
Questionnaire
- The Visual Analog Scale (VAS) is used at 0 (pre-treatment), 2 and 24 hours to register the
comfort of the materials used.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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