Lipedema
Conditions
Interventions
Group 1: Observational Study: Pain assessement before the operation, after 1 week, 6 weeks and after completion of all operations with SF-12, WHO-5, Germain Pain Questionaire und PDI. Evaluation of sk
Sponsors
BG Unfallklinik Ludwigshafen
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Female patients with diagnosed stage 1–3 lipedema and planned liposuction of the lower extremities, with at least 6 months of compression therapy.
Exclusion criteria
Exclusion criteria: Age <18 years, long-term anticoagulant medication, malignancy, lack of consent, coagulation disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain before and after the operations with NAS and questionairs (SF-12, WHO-5, PDI, German Pain Questionare) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Changes in Heamoglin, Potassium, Natrium, Leukozytes before and after the operations. -Skin sensitivity before and after operation(6 weeks after die Operation) | — |
Countries
Germany
Contacts
Public ContactChristian Witulski
BG Unfallklinik Ludwigshafen
Outcome results
None listed