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Acute Treatment and Long-term Assessment of Adult Infectious Meningitis

Study acronym: ATLAS-I
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from Hospital Israelita Albert Einstein

Record History

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  1. Primary endpoint(s) modifiedv3 Show 4 more changesShow less
    • Trial sites expanded: 3 → 6 locations
    • Eligibility criteria expanded, about 124 words
    • Secondary endpoints: 11 to 16
    • Study description expanded, about 4 words
  2. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Start date changed from estimate of Aug 2025 to Mar 30, 2026
    • Study sites: 0 to 3
    • Primary completion date: Sep 2026 to Dec 2026
    • Study completion date: Dec 2026 to Feb 2027
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Prospective, multicenter, observational clinical registry of adult patients with acute infectious meningitis across approximately 30 public and private hospitals in Brazil. The study will include adults, 18 years old and older, with suspected acute infectious meningitis. Data will be collected during hospitalization and post-discharge to evaluate clinical management, treatment and short and long-term outcomes. The study aims to generate real-world evidence on current practices and outcomes to support improvements in national care protocols.
Trial Details
NCT Number NCT07027475
Lead Sponsor Hospital Israelita Albert Einstein
Collaborators: Ministry of Health, Brazil
Conditions
(from sponsor)		 Viral Meningitis, Bacterial Meningitis, Fungal Meningitis, Meningitis
Related terms Meningitis, Meningitis, Bacterial, Meningitis, Fungal, Meningitis, Viral
Enrollment 624 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov