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Clinical Trials/NCT00790179
NCT00790179
Completed
Not Applicable

Continuous Lumbar Plexus Block for Postoperative Pain Control After Total Hip Arthroplasty

Northwell Health0 sites225 target enrollmentJanuary 2003
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ConditionsPostoperative Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Northwell Health
Enrollment
225
Primary Endpoint
VAS pain scores
Status
Completed
Last Updated
17 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

Continuous lumbar plexus and femoral blocks have been demonstrated to provide effective postoperative analgesia of the lower extremity following total joint arthroplasty. The purpose of this study was to compare these two techniques when used with intravenous patient-controlled analgesia and the use of patient-controlled analgesia alone for postoperative pain management following unilateral total hip arthroplasty.

Detailed Description

above may be applied

Registry
clinicaltrials.gov
Start Date
January 2003
End Date
March 2007
Last Updated
17 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •18-80 years old
  • •primary diagnosis of osteoarthritis

Exclusion Criteria

  • •allergy to local anesthetics
  • •peripheral neuropathy
  • •opioid dependency
  • •coagulopathy

Outcomes

Primary Outcomes

VAS pain scores

Time Frame: at 24 and 48 hours

Secondary Outcomes

  • hydromorphone consumption,patient satisfaction,distance ambulated, opioid-related side effects(at 24 and 48 hours)

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