Saphenous Nerve Block for Partial Meniscectomy
Status unconfirmed · Phase 3
Conditions studied: Pain, Joint, Pain, Procedural, Meniscectomy
In brief
Partial meniscectomy and meniscus repair are two of the most common orthopedic surgery procedures. As these procedures are being increasingly performed in ambulatory surgical centers, there has been a shift towards providing improved analgesia to ensure timely discharge, as well as preventing unwanted pain and side effects. As such, it has become common practice to use an intra-articular injection of local anesthetic to achieve post-operative pain control. However, these effects are short lived, requiring a multimodal approach to analgesia. To date, no optimal pain control strategy has been described for arthroscopic partial meniscectomy or meniscus repair. The purpose of this study is to examine the outcomes of subcutaneous saphenous nerve block with 0.5% ropivacaine at the medial femoral epicondyle/adductor hiatus plus portal 0.5% ropivacaine injection vs portal 0.5% ropivacaine injection alone for patients undergoing arthroscopic partial meniscectomy or meniscus repair.
Key facts
- Study ID
- NCT04717609
- Run by
- Rothman Institute Orthopaedics
- People needed
- 160
- Starts
- 2021-01-25
- Expected to finish
- 2022-01-25
- Last updated by the study team
- 2021-01-22
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age ≥ 18
- Scheduled for arthroscopic meniscectomy or meniscus repair
You may not qualify if…
- Multiple-ligament injury
- Primary ACL reconstruction or ACL revision reconstruction
- Articular cartilage restoration surgery
- Evidence of microfracture
- History of allergy to local anesthetics
- Pre-existing saphenous neuropathy
- Unable to be prescribed opioids due to allergy or other reason
Where it is running
- Rothman Orthopaedic Institute — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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