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ACTIVE NOT RECRUITING
NCT03655561

Lassa Fever Clinical Course and Prognostic Factors in Nigeria

Sponsor: Alliance for International Medical Action

View on ClinicalTrials.gov

Summary

The investigators propose to conduct a nationwide (Nigeria), prospective, non-interventional cohort study describing the clinical course, biological characteristics, case management and outcomes in patients hospitalized for a suspected or confirmed diagnosis of Lassa fever in tertiary medical facilities situated in the most affected Nigerian states. Special focuses will be made on situations at risk of bad outcome such as pregnancies, acute kidney injury and electrolytic imbalance in patients with confirmed Lassa fever. Participants for which the diagnosis of Lassa fever will be finally excluded by reverse-transcriptase polymerase chain reaction (RT-PCR) will constitute the control group.

Official title: Observational Cohort Study of Lassa Fever Clinical Course and Prognostic Factors in an Epidemic Context in Nigeria

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

1200

Start Date

2018-04-05

Completion Date

2025-12-31

Last Updated

2025-01-29

Healthy Volunteers

No

Interventions

OTHER

Non interventional research

Participants are receiving the standard of care according to Nigerian Center for Disease Control (NCDC) Standard Operating Procedures for Lassa fever case management. This include the administration of intravenous ribavirin for Lassa confirmed cases as well as critically-ill Lassa suspected cases.

Locations (2)

Alex Ekwueme Federal University Teaching Hospital Abakaliki

Abakaliki, Ebonyi State, Nigeria

Owo Federal Medical Centre (Owo FMC)

Owo, Ondo State, Nigeria