Influence of LymphaTouch® on perioperative swelling of the lower extremity after total knee arthroplasty implantatio

Not Applicable

• Conditions: T81.9; Unspecified complication of procedure

• Registration Number: DRKS00018837
• Lead Sponsor: Klinik und Poliklinik für Orthopädie, Uniklinik Köln

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-01-07
• Study Completion: 2021-03-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Postoperative after knee TEP and signed consent form

Exclusion Criteria

Unsigned consent form

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative swelling of the extremity via circumferential measurements of the affected limb

Secondary Outcome Measures

Name	Time	Method
1. taking painkillers<br>2. range of motion of the adjacent joints<br>3. visual analogue scale<br>4. duration of hospitalisation<br>5. WOMAC Score<br>6. KOOS