CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 4,043 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02431923
NCT02431923N/ACompleted

Partnership for Research on Ebola Virus (PREVAIL) Prevail III: Ebola Natural History Study

National Institute of Allergy and Infectious Diseases (NIAID)·observational·Posted May 1, 2015·Updated Oct 10, 2022

In Brief

An observational study for Ebola Virus Disease. Completed, enrolled 4,043 participants across 4 sites in 2 countries.

Detailed Summary

Background: \- Ebola is a lethal disease. A lot is still unknown about Ebola and its long-term effects. Researchers want to learn what ill health conditions Ebola survivors have. They want to learn if Ebola survivors can infect others in their household through close contact. They also want to learn if Ebola survivors are immune from getting Ebola again. To learn these things, they want to follow people in Liberia for 5 years. Objectives: \- To learn how Ebola affects the health of survivors and the people they live with. Eligibility: \- People in Liberia who had Ebola in the past 2 years, who share a household with someone who had Ebola, or who got ill and went to an Ebola Treatment Unit but were sent home because they did not have Ebola. Design: * Participants will be screened with family illness history, physical exam, and blood tests. They may have an eye exam. * Ebola survivors and those who went to a Treatment Unit but did not have Ebola will visit a clinic at 3, 6, and 12 months, then every 6 months for 5 years. At each visit, they will repeat the screening tests. * Participants who live with someone who had Ebola will have only the screening visit. But they may be asked to return for follow-up visits. These visits will help researchers learn more about the differences between those who have had Ebola and those who have not. * Participants brought to the NIH Clinical Center will have documentation of positive Ebola virus PCR and a clinical syndrome compatible with acute EVD. * The study will last 5 years.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesLiberia, United States
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedMay 1, 2015
Enrollment StartDec 2, 2017
Primary CompletionApr 30, 2021
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 11.2 years ago