Analgesic efficacy of saphenous nerve blockade for outpatient knee anterior cruciate ligament surgery
Completed
- Conditions
- postoperative pain
- Registration Number
- NL-OMON44745
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Informed consent, age 18-65 years, ASA status I - III, rupture of the anterior cruciate ligament.
Exclusion Criteria
Inability to perform written informed consent, contraindication for regional anesthesia, contraindication for general anesthesia, allergy against local anesthetics, BMI > 35, pre-existing diagnosed neuropathy of the operated leg, ingestion of strong opioids, pregnancy or breastfeeding status. History of significant cardiovascular disease (MI, CVA, peripheral vascular disease)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Readiness to discharge in hours and according to Post-Anesthetic<br /><br>Discharge Scoring System (PADSS)</p><br>
- Secondary Outcome Measures
Name Time Method <p>Degree of motor blockade, patient satisfaction, pain score (VAS) and overall<br /><br>benefit of analgesia score (OBAS) for the day of surgery and the first<br /><br>postoperative day.<br /><br><br /><br>- IKDC questionnaire<br /><br>- KOOS questionnaire<br /><br>- SF-12<br /><br>- Sensory blockade extent<br /><br>- Time to rescue analgesic (morphine postoperatively)<br /><br>- Total analgesic consumption (telephone interview)<br /><br>- Time to mobilization (telephone interview)<br /><br>- Knee function will be done by the Knee Society 6 weeks after surgery<br /><br>- Incidence of falls or near falls</p><br>