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Oral Dexamethasone as an Intervention for Postoperative Pain and Nausea Management in Total Knee Arthroplasty

StatusCompleted
PhasePhase 4
Started
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Record History

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  1. Primary endpoint(s) modified Show 5 more changesShow less
    • Results posted: Sep 25, 2026
    • Completed without a posted recruiting period
    • Final enrollment: 109 participants (planned 300)
    • Primary completion date changed from estimate of Jun 2022 to Sep 1, 2021
    • Eligibility criteria expanded, about 2 words
  2. Re-verified, no change to tracked fieldsv3
  3. Primary endpoints: 5 to 1v2 Show 7 more changesShow less
    • Trial status: Not Yet Recruiting to Completed
    • Enrollment target: estimated 300 to confirmed 109
    • Study sites: 0 to 1
    • Primary completion date changed from estimate of Jun 2022 to Sep 1, 2021
    • Study completion date changed from estimate of Dec 2022 to Dec 1, 2022
    • Start date changed from estimate of Jul 2020 to Aug 1, 2020
    • Secondary endpoints shortened, about 13 words
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study aims to determine if oral dexamethasone provides clinically significant improvement in postoperative outcomes, specifically nausea and pain scores.
Trial Details
NCT Number NCT04432259
Lead Sponsor Henry Ford Health System
Conditions
(from sponsor)		 Arthritis Knee, Postoperative Nausea, Postoperative Pain
Related terms Postoperative Nausea and Vomiting, Postoperative Pain
Enrollment 109 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov