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Efficacy of Epidural Steroid for Controlling Pain After Primary TKA

T

Thammasat University

Status and phase

Completed
Phase 4

Conditions

Postoperative Pain

Treatments

Drug: epidural triamsinolone
Drug: epidural lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT02001259
orthoTU05

Details and patient eligibility

About

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

Full description

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

Enrollment

108 patients

Sex

All

Ages

50 to 85 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

108 participants in 2 patient groups

Epidural lidocaine
Active Comparator group
Description:
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
Treatment:
Drug: epidural lidocaine
epidural triamsinolone
Experimental group
Description:
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
Treatment:
Drug: epidural triamsinolone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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