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Efficacy of Preoperative Intravenous Dexamethasone in Primary Total Knee Arthroplasty

NCT02102815 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2019-01-15

No results posted yet for this study

Summary

To determine efficacy of preoperative IV dexamethasone for postoperative pain control after TKA.

Conditions

  • Postoperative Pain

Interventions

DRUG

Dexamethasone

Dexamethasone 0.15mg/kg mixed with NSS up to 50 mL IV slowly push over 5 minutes

DRUG

Normal saline

NSS 50 mL IV slowly push over 5 minutes

Sponsors & Collaborators

  • Thammasat University

    lead OTHER

Principal Investigators

  • Supakit Kanitnate, M.D. · Orthopaedics department, Thammasat University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-05-31
Primary Completion
2016-02-29
Completion
2016-06-30

Countries

  • Thailand

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Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02102815 on ClinicalTrials.gov