Trials / Enrolling By Invitation
Enrolling By InvitationNCT02483260
Intravenous Ribavirin Protocol to Treat Individuals With Viral Hemorrhagic Fever
Intravenous Ribavirin Protocol to Treat Individuals With Viral Hemorrhagic Fever (Crimean-Congo Hemorrhagic Fever or Lassa Fever)
- Status
- Enrolling By Invitation
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- Sponsor
- U.S. Army Medical Research and Development Command · Federal
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Is ribavirin a therapeutic option for patients with a probable or suspected case of viral hemorrhagic fever?
Detailed description
To provide an intravenous ribavirin therapeutic option for patients with a probable or suspected case of viral hemorrhagic fever, specifically Crimean-Congo hemorrhagic fever or Lassa fever.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ribavirin | 1. Loading dose, 33 mg/kg (maximum dose: 2.64 g) 2. Followed in 6 hours by a dose of 16 mg/kg (maximum dose: 1.28 g) every 6 hours for the first 4 days (15 doses) 3. Followed by a dose of 8 mg/kg (maximum dose: 0.64 g) every 8 hours for the subsequent 6 days (18 doses). |
Timeline
- Start date
- 2016-06-16
- Primary completion
- 2027-10-01
- Completion
- 2028-12-01
- First posted
- 2015-06-26
- Last updated
- 2025-06-27
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT02483260. Inclusion in this directory is not an endorsement.