Trials / Completed
CompletedNCT00508495
Analgesic Efficacy, Safety and Tolerability of Two Paracetamol-Containing Solutions in Post-Surgical Hip Replacement Pain
Single-Dose Comparison of the Analgesic Efficacy, Safety and Tolerability of Two Paracetamol 1%-Containing Solutions and Placebo in a Post-Surgical Total Hip Replacement Model
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 148 (actual)
- Sponsor
- Baxter Healthcare Corporation · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to evaluate the therapeutic efficacy, safety and local tolerability of two different paracetamol-containing solutions in postoperative total hip replacement. They will be compared to placebo (a dummy treatment which contains no active ingredient).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Paracetamol (acetaminophen) | Four 100 mL, 15 min IV infusions at six hour intervals |
| DRUG | Paracetamol 1% solution | Four 100 mL, 15 min IV infusions at six hour intervals |
| DRUG | 0.9% sodium chloride solution | Four 100 mL, 15 min IV infusions at six hour intervals |
Timeline
- Start date
- 2007-08-01
- Primary completion
- 2008-03-01
- Completion
- 2008-03-01
- First posted
- 2007-07-30
- Last updated
- 2011-08-11
Locations
8 sites across 1 country: Hungary
Source: ClinicalTrials.gov record NCT00508495. Inclusion in this directory is not an endorsement.