Optimization of a Fast-track Concept for Knee Joint Replacement (KneeOptOut2)
Knee Arthropathy, Postoperative Pain, Postoperative Complications
About this trial
This is an interventional treatment trial for Knee Arthropathy focused on measuring ERAS, pain, knee arthroplasty, joint pain, regional anaesthesia
Eligibility Criteria
Inclusion Criteria:
• patients undergoing elective, primary knee joint replacement in combined general anaesthesia
Exclusion Criteria:
- heart insufficiency NYHA >2
- liver insufficiency > CHILD B
- evidence of diabetic polyneuropathy
- severe adipositas BMI >40
- patients < 18 years
- pregnancy
- in case of police custody
- participation in a paralleled interventional RCT in a time frame of 30 days
- chronic opioid therapy >3 months before scheduled surgery
- allergy against medication required for surgery or anaesthesia
Sites / Locations
- Charité - Universitätsmedizin Berlin
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Early-intraoperative Local infiltration technique
Late-intraoperative Local infiltration technique
A distal regional anaesthesia is performed in which the nerves are blocked by a local anaesthetic in the tissue in the immediate vicinity of the operating area ("tissue infiltration technique"). The LIA is applied in a total of 4 steps during the preparation of the knee joint: 1. after the skin incision, 2. after the capsule incision, 3. after complete exposure of the knee joint, 4. when the posterior knee capsule is reached.
A distal regional anaesthesia is performed in which the nerves are blocked by a local anaesthetic in the tissue in the immediate vicinity of the operating area ("tissue infiltration technique"). The LIA is applied after the preparation of the femur and tibia bone shortly before the prosthesis is inserted and during the retreat from the knee joint.