Randomised comparison of inpatient pain management in isolated patellofemoral replacement - pilot study
Not Applicable
Recruiting
- Conditions
- M17.1Other primary gonarthrosis
- Registration Number
- DRKS00029341
- Lead Sponsor
- Medizinische Hochschule Hannover
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Indication for primary patellofemoral replacement
- Age: 18 - 85 years
Exclusion Criteria
- Known diseases of the cardiovascular system that lead to severe limitations in exercise capacity, corresponding to NYHA3 and NYHA4.
- Known dementia
- Known drug abuse
- Intolerances and/or allergies that make participation in the study impossible.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Recording of knee joint function using torque measurement 6 weeks postoperatively to record quadriceps femoris muscle function of the 2 study groups with different analgesia regimens (LIA group, NKF group).<br>
- Secondary Outcome Measures
Name Time Method - Analgesic/opioid consumption<br>- Side effects of analgesics<br>- Complications<br>- Patient satisfaction<br>- Length of hospital stay<br>- Assessment of chronic pain status<br>