I87.2 I83.2
Conditions
Interventions
Group 1: All patients who are suitable for the study after checking the inclusion and exclusion criteria take part. The study participants wear both compression stockings to be compared one after the
Sponsors
Bauerfeind AG - Phlebology Business Development & Medical Affairs
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Patients between 18 and 85 years CVI in stage according to CEAP C5 and C6
Exclusion criteria
Exclusion criteria: Known contraindications to wearing the compression stocking (e.g. intolerance to the compression material advanced heart failure)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lower leg volume measured at the beginning and end of the wearing phases using 3D-assisted volume reconstruction of the legs (BT 610) | — |
Secondary
| Measure | Time frame |
|---|---|
| Before and after each wearing phase, the following data are collected: 1. wearing comfort (questionnaire) 2. volume change of the thigh (BT 610) 3. frequency of adverse events (questionnaire) 4. quality of life (SF36, Tübingen Quality of Life Questionnaire, DLQI) | — |
Countries
Germany
Contacts
Public ContactMichael Jünger
Klinik und Poliklinik für Hautkrankheiten der Universität Greifswald
Outcome results
None listed