Trials / Completed
CompletedNCT00286065
Study to Determine Efficacy and Safety of Inhaled AeroLEF in the Treatment of Acute Post-op Pain in Adult Patients Undergoing Elective Orthopedic Surgery
Multi-Centre Placebo-Controlled Randomized 2 Part Study to Determine Efficacy and Safety of Inhaled AeroLEF in the Treatment of Acute Post-Op Pain in Adult Patients Undergoing Elective Orthopedic Surgery
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 123 (planned)
- Sponsor
- YM BioSciences · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the effect of pain relief with AeroLEF in adult patients, following orthopedic surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AeroLEF |
Timeline
- Start date
- 2006-01-01
- First posted
- 2006-02-02
- Last updated
- 2007-06-27
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT00286065. Inclusion in this directory is not an endorsement.