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
| Type | Name | Description |
|---|---|---|
| DRUG | etoricoxib | etoricoxib 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.