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Starting soon Observational

Study of Filovirus Disease Morbi-mortality

NCT07821580 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-09
Last updated
2026-09-16

Condition(s) studied

Filovirus Disease

Study summary

Filoviruses, including Ebola and Marburg, cause hemorrhagic fevers associated with high mortality and still limited scientific literature, in particular for some rare species such as the Bundibugyo virus. The current epidemic of Bundibugyo virus disease in the Democratic Republic of the Congo (DRC) and Uganda, which has been declared a public health emergency of international concern by the World Health Organization (WHO), illustrates the importance of better characterizing this infection, whose genetic specificities complicate the transposition of diagnostic, therapeutic and vaccine tools developed for Ebola Zaire.

Given the incubation time of filoviruses and international mobility, cases can be diagnosed and managed outside of epidemic areas, including in exposed caregivers. However, clinical, biological and therapeutic knowledge available in this context remain very limited.

This situation justifies the implementation of an observational cohort of patients with a confirmed filovirus disease, who have arrived or were diagnosed in France.

This cohort will describe the clinical evolution of the disease, its prognosis and its pathophysiology, as well as identify new diagnostic, therapeutic or preventive leads.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion criteria : * Confirmed filovirus disease * Hospitalized in a Referenced Healthcare Facility in France Non inclusion criteria : * Refusal by the patient or their legal representative to sign the consent form for the study * Patient deprived of their liberty or subject to a legal protection measure

Primary outcome measure(s)

  • Vital status on day 28. — 28 days
    The objective is to describe mortality at day 28 in patients with confirmed filovirus diseases. Day 1 is the day of the first documented positive PCR, regardless of the location of the PCR.

Trial sites (1)

FacilityCityRegionStatus
Hôpital Saint Antoine Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07821580 on ClinicalTrials.gov ↗ ← All trials in France