I89.0
Conditions
Interventions
Group 1: JPM and PicoPress devices are applied simultaneously at anatomical measurement point B1 under adaptive compression wraps. Data collection are performed in a sequence, starting with resting pr
Sponsors
Charité Universitätsmedizin Berlin, Arbeitsbereich Physikalische Medizin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Unilateral or bilateral lymphedema of the extremities - Stage II or III - Currently undergoing compression therapy - Trained in the use of adjustable compression wraps - Sufficient manual and sensory function to use adjustable compression wraps - Sufficient verbal comprehension and cognitive ability to participate in the study - Willingness to participate in the study and provide informed consent
Exclusion criteria
Exclusion criteria: - Significant changes in circumference or anatomical deviations from the approximate physiological circumference at measurement point B1 at the junction of the Achilles tendon and the gastrocnemius muscle due to lymphedema - Contraindications or intolerance to compression therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of compression pressure readings (resting pressure in mmHg) between the Juzo Pressure Monitor (JPM) and PicoPress system, | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of pressure readings: - maximum working pressure (mmHg) - venous filling pressure while standing (mmHg) - Static Stiffnes Index (SSI) - measurement deviation different standardized pressure applications | — |
Countries
Germany
Contacts
Public ContactAnett Reißhauer
Charité Universitätsmedizin Berlin, Arbeitsbereich Physikalische Medizin
Outcome results
None listed