Driving Reduced AIDS-associated Meningo-encephalitis Mortality

NCT03226379 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 495

Last updated 2022-05-04

No results posted yet for this study

Summary

The DREAMM project is investigating whether the DREAMM interventions (1) Health system strengthening, 2) Co-designed education programs tailored to frontline healthcare workers, 3) Implementation of a diagnostic and treatment algorithm and, 4) Communities of practice in infectious diseases and laboratory capacity building) when combined reduce two week all-cause mortality of HIV-associated meningo-encephalitis in African LMICs.

Conditions

  • AIDS-Related Opportunistic Infections
  • Meningo-encephalitis
  • Cryptococcal Meningitis
  • Bacterial Meningitis
  • Tuberculous Meningitis
  • Cerebral Toxoplasmosis

Interventions

OTHER

DREAMM

4 DREAMM interventions to reduce HIV-related meningoencephalitis mortality once access to essential diagnostic tests and medicines: 1. Health system strengthening 2. Delivery of a co-designed education program tailored to frontline healthcare workers 3. Implementation of an algorithm for HIV-related meningoencephalitis 4. Infectious diseases/AHD mentorship and laboratory capacity building

Sponsors & Collaborators

  • European and Developing Countries Clinical Trials Partnership (EDCTP)

    collaborator OTHER_GOV
  • National Agency for Research on AIDS and Viral Hepatitis (ANRS)

    collaborator OTHER
  • Institut Pasteur

    collaborator INDUSTRY
  • National Institute for Medical Research, Tanzania

    collaborator OTHER_GOV
  • Amana Hospital, Dar es Salaam, Tanzania

    collaborator UNKNOWN
  • University of North Carolina Project-Malawi (UNC Project), Lilongwe, Malawi

    collaborator UNKNOWN
  • Kamuzu Central Hospital

    collaborator OTHER
  • Yaounde Central Hospital

    collaborator OTHER_GOV
  • Zomba Central Hospital, Zomba, Malawi

    collaborator UNKNOWN
  • Lighthouse Trust

    collaborator OTHER
  • Mwananyamala Hospital, Dar es Salaam, Tanzania

    collaborator UNKNOWN
  • St George's, University of London

    lead OTHER

Principal Investigators

  • Angela Loyse, MD · St George's, University of London

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-23
Primary Completion
2021-04-30
Completion
2021-09-30

Countries

  • Cameroon
  • Malawi
  • Tanzania

Study Locations

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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 NCT03226379 on ClinicalTrials.gov