MedTrace Logo

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

NCT06438133 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 52

Last updated 2025-12-26

No results posted yet for this study

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.

Conditions

  • Compression; Vein
  • Venous Insufficiency
  • Lymphedema of Leg
  • Digital Technology

Interventions

OTHER

CIMON

The sensor assess changes in the circumference of the limb and will be applied to the lower limb before compression bandaging is applied.

OTHER

Sens Motion

The sensor assess physical activity and the amount of time spent at rest, standing, walking, running and count steps.

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER

  • Bispebjerg Hospital

    collaborator OTHER

  • Odense University Hospital

    collaborator OTHER

  • Copenhagen University Hospital, Hvidovre

    collaborator OTHER

  • Carsten Bogh Juhl

    lead OTHER

Principal Investigators

  • Carsten Bogh Juhl, Professor · Herlev and Gentofte Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-10
Primary Completion
2025-12-18
Completion
2025-12-18

Countries

  • Denmark

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06438133 on ClinicalTrials.gov