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Clinical Trials/NCT01447277
NCT01447277
Completed
Not Applicable

The Addition of a Preoperative Sciatic Nerve Block to a Femoral Nerve Block for Ambulatory Arthroscopic ACL Reconstruction

University of California, San Francisco1 site in 1 country68 target enrollmentOctober 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anterior Cruciate Ligament Tear
Sponsor
University of California, San Francisco
Enrollment
68
Locations
1
Primary Endpoint
Pain Scores
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The investigators propose that a preoperative femoral and sciatic blocks vs a femoral block only, prior to ambulatory anterior cruciate ligament (ACL) reconstruction will lead to a decrease in opiate consumption, pain scores, and post-anesthesia care unit (PACU) length of stay. The investigators are prospectively randomizing patients to either a femoral or a fem/sciatic block and monitor outcomes.

Detailed Description

Although femoral nerve blocks improve analgesia after anterior cruciate ligament (ACL) reconstruction, patients often complain of posterior knee pain, which can be treated with a sciatic nerve block. In a prospective randomized study, we compare preoperative femoral nerve block to a combined femoral and sciatic block in patients undergoing ambulatory ACL reconstruction. We hypothesize that the combined femoral/sciatic nerve block patients would have improved analgesia, fewer opioid-related side effects, and shorter PACU length of stay and improved patient satisfaction.

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
June 2013
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 18 and over
  • ASA status I-II
  • Scheduled for ambulatory Arthroscopic ACL Surgery

Exclusion Criteria

  • Allergy to Local anesthetics or opiates used in the study
  • Contraindications for regional anesthesia
  • coagulopathy, anticoagulation, Thrombocytopenia
  • infection at site of injection
  • Chronic pain and high preoperative opiate requirements
  • High risk for PONV

Outcomes

Primary Outcomes

Pain Scores

Time Frame: PACU and POD1, 2 and 3.

Secondary Outcomes

  • Length of stay(Duration of stay in the recovery room)
  • Opiate consumption(During surgery, recovery room and for 3 days after discharge)
  • PONV(During the recovery room stay and after discharge from surgery center for up to 3 days.)

Study Sites (1)

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