# An Efficacy and Safety Study of Periarticular Parecoxib Sodium for Pain Management in Total Knee Arthroplasty

> **NCT01311804** · PHASE3 · UNKNOWN · sponsor: **Ministry of Health, Malaysia** · enrollment: 125 (estimated)

## Conditions studied

- Unilateral Primary Osteoarthritis of Knee

## Interventions

- **PROCEDURE:** parecoxib sodium
- **PROCEDURE:** parecoxib sodium

## Key facts

- **NCT ID:** NCT01311804
- **Lead sponsor:** Ministry of Health, Malaysia
- **Sponsor class:** OTHER_GOV
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2011-04
- **Primary completion:** 2011-04
- **Final completion:** 2011-10
- **Target enrollment:** 125 (ESTIMATED)
- **Last updated:** 2011-03-10


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01311804

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01311804, "An Efficacy and Safety Study of Periarticular Parecoxib Sodium for Pain Management in Total Knee Arthroplasty". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01311804. Licensed CC0.

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