Meningitis: Burden, Causes, Screening and Prevention in Rural Northern Uganda

NCT05496673 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11100

Last updated 2026-01-12

No results posted yet for this study

Summary

This study will investigate the burden, causes, diagnostics, treatments and preventive measures related to meningitis in northern Uganda. We hypothesize that understanding the burden of meningitis, risk factors, diagnostics, treatments and the preventive measures will provide information regarding the gaps in care that can be addressed in order to improve the continuum of meningitis care. we hypothesize that our data will support the advocacy for the implementation of routine vaccination for the prevention of bacterial meningitis and improving guidelines for Cryptococcal antigen (CrAg) screening for prevention of cryptococcal meningitis, which will save lives in Uganda.

Aim 1: To prospectively collect data on 1100 patients with meningitis and meningitis symptoms who were admitted to Lira Regional Referral Hospital (LRRH) to assess burden, etiologies, pathogenesis, and outcomes of meningitis using modern diagnostic testing not previously available in Uganda.

Aim 2: To perform CrAg screening of 10,000 HIV-positive patients to determine the prevalence of cryptococcal antigenemia (infection) and conduct a case control study to compare risk factors and outcomes among CrAg-positive patients and matched CrAg-negative controls based on age, sex, TB status, ART experience, CD4 count, and viral load.

Conditions

Interventions

DIAGNOSTIC_TEST

Pastorex Latex Agglutination Test

Rapid diagnosis of bacterial meningitis

DIAGNOSTIC_TEST

Biofire PCR for meningitis

Rapid diagnosis of multiple forms of meningitis

DIAGNOSTIC_TEST

Immy CrAg Lateral Flow Assay

Rapid diagnosis of cryptococcal meningitis

Sponsors & Collaborators

  • Lira University

    collaborator OTHER
  • Fogarty International Center of the National Institute of Health

    collaborator NIH
  • Makerere University

    collaborator OTHER
  • University of Rochester

    lead OTHER

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-01
Primary Completion
2031-09-01
Completion
2031-09-01

Countries

  • Uganda

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05496673 on ClinicalTrials.gov