Trials / Completed
CompletedNCT01037192
Evaluating the Use of Large-dose, Extended Interval Vancomycin Intravenous Administration for Skin and Soft Tissue Infections
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 4 (actual)
- Sponsor
- Fraser Health · Academic / Other
- Sex
- All
- Age
- 19 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Our hypothesis is that large-dose, extended-interval vancomycin (30 mg/kg IV q24h) administration provides non-inferior clinical efficacy and microbiological efficacy to standard vancomycin (15 mg/kg IV q12h) administration for skin and soft tissue infections in an outpatient setting.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | vancomycin | vancomycin 30 mg/kg intravenous administered once daily |
| DRUG | vancomycin | vancomycin 15 mg/kg intravenous administered twice daily (standard dosing) |
Timeline
- Start date
- 2010-03-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2009-12-22
- Last updated
- 2015-08-27
- Results posted
- 2011-07-08
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT01037192. Inclusion in this directory is not an endorsement.