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Clinical Trials/NCT01108562
NCT01108562
Withdrawn
Phase 1

Treatment of Postoperative Pain After Total Hip Arthroplasty Using Intravenous Lidocaine Infusion in Combination With Patient Controlled Analgesia: a Prospective Randomized, Double-blinded, Placebo-controlled Study

Loma Linda University0 sitesFebruary 2008

Overview

Phase
Phase 1
Intervention
Normal Saline
Conditions
Postoperative Pain Management After Total Hip Arthroplasty
Sponsor
Loma Linda University
Primary Endpoint
We propose to test the hypothesis that adding a low dose lidocaine infusion to patient controlled analgesia will lower the amount of opioids that these patients will receive, thereby improving patient safety while still providing adequate analgesia.
Status
Withdrawn
Last Updated
11 years ago

Overview

Brief Summary

This study will focus on patients undergoing total hip arthroplasty and Loma Linda University Medical Center & East Campus. These patients will be randomized to receive a low dose lidocaine infusion or placebo, in addition to the patient controlled analgesia pump. These groups will be compared to one another statistically to determine which group shows the safest and most satisfying pain control.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
August 2008
Last Updated
11 years ago
Study Type
Interventional
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult male or female undergoing a total hip arthroplasty Subject is American Society of Anesthesiologists physical status 1, 2, or 3 Subject has voluntarily signed and dated the informed consent document approved by the IRB Be English speaking

Exclusion Criteria

  • Age \> 80 years old or younger than 18 years old Congestive heart failure Hepatic insufficiency Neurological disorders Psychiatric disorders Steroid treatment No history of atrial fibrillation Chronic pain disorder with opioid treatment

Arms & Interventions

Control Group

Patients will receive a Dilaudid PCA in combination with a placebo infusion of normal saline.

Intervention: Normal Saline

Lidocaine Group

Patients will be receive a Dilaudid PCA in combination with a continuous Lidocaine infusion.

Intervention: Lidocaine

Outcomes

Primary Outcomes

We propose to test the hypothesis that adding a low dose lidocaine infusion to patient controlled analgesia will lower the amount of opioids that these patients will receive, thereby improving patient safety while still providing adequate analgesia.

Time Frame: 24 hours

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