Clinical Trials Directory

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

TypeNameDescription
DRUGRibavirin1. 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.