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Ceftriaxone Dosage for Non-Critical Community-Acquired Pneumonia

Study acronym: DC-CAP
StatusNot Yet Recruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from University of Maryland, Baltimore

Record History

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  1. Notable Primary endpoint(s) modified
    • Enrollment increased: 430 → 900 participants
    • Study sites: 2 to 4
    • Secondary endpoints: 11 to 9
    v2
  2. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Aim: Demonstrate the equivalent efficacy and superior safety of Ceftriaxone 1 gram daily compared with Ceftriaxone 2 grams daily among hospitalized patients with community-acquired pneumonia who are not admitted to the intensive care unit.\<p\> Hypothesis: Among hospitalized patients outside of the intensive care unit with community-acquired pneumonia who are prescribed Ceftriaxone, a dosage of 1 gram daily will be associated with an equivalent rate of clinical cure and fewer adverse events than a dosage of 2 grams daily.
Trial Details
NCT Number NCT07537413
Lead Sponsor University of Maryland, Baltimore
Conditions
(from sponsor)
Community Acquired Pneumonia (CAP)
Related terms Community-Acquired Pneumonia
Enrollment 900 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov