Clinical Trials Directory

Trials / Terminated

TerminatedNCT00763685

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

Double-Blind, Randomized, Placebo -Controlled 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

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
East Tallinn Central Hospital · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Primary Hypothesis: 1\. The analgesic effect of etoricoxib 120 mg administered 1 hour preoperatively is greater than that of placebo in the treatment of postoperative pain.

Conditions

Interventions

TypeNameDescription
DRUGetoricoxibetoricoxib 120 mg, paracetamol 1 g

Timeline

Start date
2010-06-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2008-10-01
Last updated
2012-01-31

Locations

1 site across 1 country: Estonia

Source: ClinicalTrials.gov record NCT00763685. Inclusion in this directory is not an endorsement.