Clinical Trials Directory

Trials / Completed

CompletedNCT02604550

Anterior Cruciate Ligament Pain Study

Comparison Between Femoral Nerve Block and Adductor Canal Block for Anterior Cruciate Ligament Reconstruction: A Prospective Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
115 (actual)
Sponsor
Emory University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The objective of this study is to compare the pain control benefit of two different types of nerve blocks in patients undergoing anterior cruciate ligament (ACL) reconstruction.

Detailed description

This trial is a prospective, randomized, surgeon-blinded, two-armed trial to investigate the safety and efficacy of femoral nerve blocks versus adductor canal blocks for participants undergoing outpatient anterior cruciate ligament (ACL) reconstruction surgery. The objective of this study is to compare the pain control benefit of two different types of nerve blocks. Ropivacaine, which is FDA-approved for use in both femoral nerve blocks as well as adductor canal blocks, will be utilized. The study will be comparing the efficacy between FDA approved treatments.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0.5%Ropivacaine 0.5% will be administered to the femoral nerve or adductor canal.
DRUGPercocet 7.5/325Percocet 7.5/325 will taken as needed up to every four hours.
DRUGNaprosyn 500 mgNaprosyn 500 mg will be taken twice daily.

Timeline

Start date
2015-11-01
Primary completion
2016-04-01
Completion
2016-04-01
First posted
2015-11-13
Last updated
2017-05-31
Results posted
2017-05-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02604550. Inclusion in this directory is not an endorsement.