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NCT05514197

The Impact of Intravenous Vitamin C Combined With Nerve Blocks on Postoperative Pain and Recovery After Total Knee Arthroplasty

Completed NA Last updated 19 November 2025
What this trial tests

NA trial testing Ascorbic acid 100mg/kg, Maximus 10g in Ascorbic Acid in 73 participants. Completed in 11 January 2024.

Timeline
2 November 2022
Primary endpoint
13 December 2023
11 January 2024

Quick facts

Lead sponsorChimei Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment73
Start date2 November 2022
Primary completion13 December 2023
Estimated completion11 January 2024
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Chimei Medical Center

Who can join

Adults 50 to 80, any sex, with Ascorbic Acid or Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this prospective randomized-control study was to evaluate the impact of a single high-dose intravenous vitamin C added to ultrasound-guided blocks at induction on postoperative pain, sngception and early functional rehabilitation of the knee joint in patients under-going total knee arthroplasty.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Chimei Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05514197.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing