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Clinical Trials/NCT02001259
NCT02001259
Completed
Phase 4

Efficacy of Epidural Steroid in Controlling Postoperative Pain After Primary Total Knee Arthroplasty: A Randomized Double-blinded Controlled Trial

Thammasat University1 site in 1 country108 target enrollmentJanuary 2014

Overview

Phase
Phase 4
Intervention
epidural lidocaine
Conditions
Postoperative Pain
Sponsor
Thammasat University
Enrollment
108
Locations
1
Primary Endpoint
post-operative pain
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to determine efficacy of epidural steroid for postoperative pain control after TKA

Detailed Description

Epidural triamsinolone can reduce postoperative pain and longer duration of pain control after TKA

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
October 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Supakit Kanitnate

orthopaedic department

Thammasat University

Eligibility Criteria

Inclusion Criteria

  • osteoarthritis of the knee who undergoing unilateral primary total knee arthroplasty
  • 50-85 years old
  • ASA class 1-3

Exclusion Criteria

  • unable to perform epidural anaesthesia
  • history of drug allergies: lidocaine, steroid
  • renal impairment (CrCl \<30 mL/min)
  • liver impairment
  • cognitive function disorders
  • displacement of epidural catheter

Arms & Interventions

Epidural lidocaine

epidural lidocaine: 3 mL of 1% lidocaine with adrenaline and 3 mL of 1% lidocaine without adrenaline into epidural catheter at 48 hr after surgery

Intervention: epidural lidocaine

epidural triamsinolone

epidural triamsinolone: 40 mg of triamsinolone (1 mL), 2.5 mL of 1% lidocaine with adrenaline and 2.5 mL of 1% lidocaine without adrenaline into epidural catheter at 48 hr after surgery

Intervention: epidural triamsinolone

Outcomes

Primary Outcomes

post-operative pain

Time Frame: 3 months

measured with VAS for pain (VAS at rest and on motion)

Secondary Outcomes

  • functional knee score(3 months)

Study Sites (1)

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