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Perineural Dexamethasone for Continuous Femoral Nerve Block

Y

Yonsei University Health System (YUHS)

Status

Completed

Conditions

Total Knee Arthroplasty

Treatments

Procedure: dexamethasone group
Procedure: sham group

Study type

Interventional

Funder types

Other

Identifiers

NCT05487001
3-2022-0230

Details and patient eligibility

About

An alternative to improve the quality of postoperative analgesia is to use various perineural adjuvants applicable to peripheral nerve block along with local anesthetics to increase the analgesic effect. Dexamethasone is a strong and long-acting corticosteroid, which reduces postoperative nausea and vomiting and increases the duration of nerve blockade. Most of the existing clinical studies compared the analgesic effect with the placebo group after adding an adjuvant in a single shot nerve block, and there were very few cases of comparing the analgesic effect with the placebo group after adding the adjuvant in peripheral nerve block through continuous catheter infusion. Therefore, we designed this study to investigate whether the use of dexamethasone as a peripheral adjuvant for continuous femoral nerve block has a better pain and recovery profile.

Enrollment

18 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients 19 years of age or older who are expected to undergo unilateral hip arthroplasty
  2. ASA PS 1-3

Exclusion criteria

  1. Revision total hip arthroplasty
  2. Allergy to drugs used in the study
  3. Patients with moderate or more hepatic impairment (AST/ALT is more than 2.5 times the upper limit of normal)
  4. Estimated glomerular filtration rate < 30 mL/min/1.73m2
  5. Opioid dependence
  6. Prolongation of PT and aPTT more than twice the upper limit of normal
  7. Pre-existing neurological or anatomical disorders of the lower extremities
  8. Serious psychiatric disorders

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

18 participants in 2 patient groups

dexamethasone group
Experimental group
Description:
a iliopsoas plane block before surgery
Treatment:
Procedure: dexamethasone group
sham group
Sham Comparator group
Description:
sham block before surgery
Treatment:
Procedure: sham group

Trial contacts and locations

1

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Central trial contact

Myoung Hwa kim

Data sourced from clinicaltrials.gov

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