Trials / Completed
CompletedNCT02269969
Once Daily Aminoglycoside Pharmacokinetics and Optimal Dosing in the Burn Population: A Prospective Study
- Status
- Completed
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Sandra Walker · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Effective antimicrobial use in the burn population is important since this population is at an increased risk for infections during their stay in hospital as a result of their burn injury. Tobramycin is an antibiotic that has activity against common burn wound associated pathogens, such as Pseudomonas Aeruginosa, and its use is becoming increasingly relevant due to the increased incidence of bacterial resistance to currently utilized antibiotics. Once daily dosing of tobramycin has been safely and effectively used in the majority of infected patients for many years with the proposed benefits of optimized antibacterial activity and reduced nephrotoxicity compared to traditional dosing. But, the once daily dosing regimen has yet to be validated in the burn population. The purpose of this study is to validate the plausibility of once daily tobramycin dosing in the burn population with intent to determine a safe, effective, and efficient dosing regimen for this population.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Tobramycin |
Timeline
- Start date
- 2015-03-01
- Primary completion
- 2015-12-01
- Completion
- 2015-12-01
- First posted
- 2014-10-21
- Last updated
- 2015-12-14
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT02269969. Inclusion in this directory is not an endorsement.