drugset / Trial / NCT03729258
Efficacy and Safety of Modified Release Cefpodoxime Formulation in the Treatment of Acute Sinusitis.
RandomizedParallel-groupDouble-blindTreatment
Summary
The aim of this study is to compare the efficacy and safety of cefpodoxime 200 mg immediate (b.i.d) and cefpodoxime 400 mg modified release (q.d) tablet formulations in the treatment of acute bacterial rhinosinusitis.
Timeline
- Start
- 2019-05-15
- Primary completion
- 2023-10-01
- Completion
- 2023-12-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Cefpodoxime | Small molecule | 200 mg | — |
| Comparator | Cefpodoxime | Small molecule | 400 mg | — |