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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 weeks
Treatment ~ Varies
Follow Up ~8 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 8 weeks for reporting.

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)

Find a Location

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
~41 spots leftby Sep 2025