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Clinical Trial Summary

Patients with chronic edema of the lower limb referred to compression bandaging in a hospital setting will be invited to participate in the validation study of a novel sensor (CIMON), which have been developed for assessing the effect of compression bandaging. Participants will have the sensor applied to the lower limb before initiation of compression bandaging and will receive usual compression treatment according to severity of the edema and usual practice at the treatment site. Duration of participation is 14 days.


Clinical Trial Description

The CIMON sensor is developed with the purpose of monitoring the effectiveness of compression bandaging (CB) in patients with chronic edema by application to the widest circumference of the calf. CIMON measures the difference in capacitance by stretching the circumferential sensor. Data from the sensor is transferred by Bluetooth technology to a secured webserver, where healthcare professionals can monitor the effect of compression bandaging. The study aims to assess the psychometric properties of the CIMON (reliability, validity and responsiveness) and assess the correlation between edema reduction and physical activity during compression bandaging. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06438133
Study type Observational
Source Herlev and Gentofte Hospital
Contact Merete Celano Wittenkamp, MPH
Phone +93911784
Email merete.celano.wittenkamp@regionh.dk
Status Not yet recruiting
Phase
Start date June 2024
Completion date December 2025

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