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Decongestive therapy with foam upholstery material

Decongestive therapy with foam upholstery material

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012982
Enrollment
62
Registered
2017-09-19
Start date
2017-09-04
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ICD10: I89.01 - Lymphedema of the upper and lower extremity, Stadium II ICD10: I89.02 - Lymphedema of the upper and lower extremity, Stadium III

Interventions

Group 1: Complex Physical Decongestion (CPD) therapy Phase I of arm lymphedema with SoftCompress©: Daily manual lymph drainage and compression bandaging with SoftCompress©-upholstery material, usually

Sponsors

Charité Universitätsmedizin Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age >18 Secondary arm lymphedema at least stadium II Indication of CPD Phase I Sufficient language skills and mental health to take part in the study Willingness to take part in the study and informed consent

Exclusion criteria

Exclusion criteria: Expected incompliance Present absolute or relative contraindications against CPD Contraindications against parts of the CPD Advanced malignant disease with expected study-drop-out (palliative CPD) Edema of unknown origin

Design outcomes

Primary

MeasureTime frame
Volume reduction in % to output value (Perometer measurement), measured directly before the first and after the last treatment.

Secondary

MeasureTime frame
- Therapeutic success: Change in feeling of tension in %; Number of improved cases; Volume reduction at point of maximum side difference; Velocity of volume reduction - Side effects: Slipping or constriction of the bandage and consequential early unwinding; wearing comfort - Economic/ ecologic effects: Duration usage of usual care-material vs. SoftCompress; Overall material comsumption All data are collected directly before and once again after the last treatment.

Countries

Germany

Contacts

Public ContactMax Liebl

Arbeitsbereich Physikalische MedizinCharité Universitätsmedizin Berlin

max.liebl@charite.de030 450 517 096

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026