Clinical trial
Efficacy and Safety of Intravenous Acetaminophen Over 48 Hrs for the Treatment…
NCT00399568 · Mallinckrodt, Industry · Completed
Key facts
| NCT number | NCT00399568 |
|---|---|
| Title | Efficacy and Safety of Intravenous Acetaminophen Over 48 Hrs for the Treatment of Post-op Pain After Gynecologic Surgery |
| Official title | Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel, Multiple-Dose Study of the Analgesic Efficacy and Safety of IV Acetaminophen (APAP) Versus Placebo Over 48 Hours(Hrs) for the Treatment of Postoperative Pain After Gynecologic Surgery |
| Lead sponsor | Mallinckrodt, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Postoperative Pain, Hysterectomy |
| Intervention type | Drug |
| Interventions | IV Acetaminophen, IV Placebo 100 mL solution |
| Enrollment | 331 |
| Start date | Nov 1, 2006 |
| Primary completion | Sep 1, 2007 |
| Completion | Sep 1, 2007 |
| First posted | Nov 15, 2006 |
| Last update posted | Oct 21, 2016 |
| Countries | United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: