# Study to Evaluate the Efficacy of Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in the Treatment of Postoperative Pain in Patients Undergoing Gynaecologic Laparoscopic Surgery

> **NCT00763685** · PHASE4 · TERMINATED · sponsor: **East Tallinn Central Hospital** · enrollment: 40 (actual)

## Conditions studied

- Pain

## Interventions

- **DRUG:** etoricoxib

## Key facts

- **NCT ID:** NCT00763685
- **Lead sponsor:** East Tallinn Central Hospital
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2010-06
- **Primary completion:** 2011-11
- **Final completion:** 2011-11
- **Target enrollment:** 40 (ACTUAL)
- **Why stopped:** The gynecological laparoscopic surgery transition to day surgery made following the study protocol not possible.
- **Last updated:** 2012-01-31

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00763685

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00763685, "Study to Evaluate the Efficacy of Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in the Treatment of Postoperative Pain in Patients Undergoing Gynaecologic Laparoscopic Surgery". Retrieved via AI Analytics 2026-09-08 from https://api.ai-analytics.org/clinical/NCT00763685. Licensed CC0.

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