Digital Supported Compression Bandaging in Patients with Chronic Edema in the Lower Limbs - Assessment of Measurement Properties of a Novel Sensor

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Other
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Chronic edema of the lower limb

• Referred to compression bandaging

• Circumference of widest point of the lower leg between 35-75 cm

Locations
Other Locations
Denmark
Department of Dermatology, Frederiksberg Bispebjerg Hospital
RECRUITING
Bispebjerg
Department of Physiotherapy and Occupational Therapy, Rigshospitalet
RECRUITING
Copenhagen
Department of Physiotherapy and Occupational Therapy, Herlev and Gentofte Hospital
RECRUITING
Herlev
Department of Physiotherapy and Occupational Therapy, Amager Hvidovre Hospital
RECRUITING
Hvidovre
Department of Oncology, Unit of Lymphedema care, Odense University Hospital Svendborg
RECRUITING
Odense
Contact Information
Primary
Merete Celano Wittenkamp, MPH
merete.celano.wittenkamp@regionh.dk
+004593911784
Backup
Carsten Bogh Juhl, Professor
carsten.bogh.juhl@regionh.dk
Time Frame
Start Date: 2024-06-10
Estimated Completion Date: 2026-12
Participants
Target number of participants: 50
Treatments
Patients with chronic edema of the lower limbs
Patients with chronic edema of the lower limbs referred to compression bandaging in a hospital setting.
Related Therapeutic Areas
Sponsors
Collaborators: Bispebjerg Hospital, Odense University Hospital, Copenhagen University Hospital, Hvidovre, Rigshospitalet, Denmark
Leads: Carsten Bogh Juhl

This content was sourced from clinicaltrials.gov