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Local Anesthetic
Pre-operative femoral nerve catheter for Postoperative Pain
Phase 3
Waitlist Available
Research Sponsored by Rothman Institute Orthopaedics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 weeks
Awards & highlights
Summary
This trial is evaluating whether a single injection of liposomal bupivacaine (Exparel) into the adductor canal is a safe and effective alternative to a femoral nerve catheter for post-operative pain control in patients undergoing ACL reconstruction.
Eligible Conditions
- Anterior Cruciate Ligament (ACL)
- Postoperative Pain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Patient satisfaction
Post operative pain management
Trial Design
2Treatment groups
Active Control
Group I: Pre-operative femoral nerve catheterActive Control4 Interventions
participants undergoing ACL reconstruction surgery will receive a femoral prior to their surgery
Group II: Pre-operative adductor canal block with liposomal bupivacaineActive Control4 Interventions
participants undergoing ACL reconstruction surgery will receive a nerve block using liposomal Bupivacaine (Exparel)
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Who is running the clinical trial?
Rothman Institute OrthopaedicsLead Sponsor
122 Previous Clinical Trials
21,550 Total Patients Enrolled
3 Trials studying Postoperative Pain
523 Patients Enrolled for Postoperative Pain
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