anterior cruciate ligament rupture
Conditions
Interventions
Identification of the adductor channel using ultrasonic landmarks such as the
femoral artery and the sartorius muscle. When a patient is randomized in the
intervention group
10 ml of Levobupivacaine 0.25% will be added in the
adductor channel. When randomized in the control group: 10 ml of sodium
chloride 0.9% (placebo) will be added in the adductor channel.
Sponsors
Sint Antonius Ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - ASA classification 1-3 - Age >= 18 years - Anterior cruciate ligament surgery - General anesthesia - Informed consent
Exclusion criteria
Exclusion criteria: - Contraindication to local anesthetics - Neuromuscular disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is postoperative pain (numerical rating score) within the first 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are pain score 48 hours postoperative, motor block result, use of postoperative pain medication including opiates and the use of rescue medication, postoperative pain location, postoperative nausea and vomiting, use of anti-emetics, overall patient satisfaction, contact within 48 hours after surgery with general practicioner or emergency department and adverse events. | — |
Countries
Netherlands
Outcome results
None listed