drugset / Trial / NCT01008007
Viusid in Adults With Acute Fever of Viral Etiology
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of the study is to assess the safety and effect of Viusid (bags of 4 grams) administration in the treatment of acute fever of viral etiology as diagnosed by clinical, hematologic and serologic parameters. The duration of this open and randomized phase 2 clinical trial will be 6 days. The estimated number of persons with acute fever of viral etiology to be recruited and randomized for the study is 200. The primary outcome measure: platelet, leukocyte and granulocyte count will be assessed at the beginning and the end of the study.
Timeline
- Start
- 2009-09
- Primary completion
- 2010-05
- Completion
- 2010-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Viusid | Unknown | 4 g | Oral |
| Comparator | Dimenhydrinate | Small molecule | 50 mg | Intramuscular |
| Comparator | dipyrone | Unknown | 600 mg | Intramuscular |
Indications
No indication recorded.