CompletedNot Applicable

Digital Supported Compression Bandaging in Patients With Chronic Edema in the Lower Limbs

Denmark52 participantsStarted 2024-06-10

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Chronic edema of the lower limb * Referred to compression bandaging * Circumference of widest point of the lower leg between 35-75 cm Exclusion Criteria: * Wounds at the lower leg (at the widest circumference of the lower leg) * Acute deep venous thrombosis in the leg * Untreated cellulitis * Severe heart- or kidneyfailure * Severe peripheral neuropathy in the lower limbs

What they're measuring

Edema reduction

Timeframe: 14 days

Trial details

NCT IDNCT06438133

SponsorCarsten Bogh Juhl

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-12-18

View on ClinicalTrials.gov More Compression; Vein trials