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The Application of Different Sedation Protocols in ICU Patients With Severe Pneumonia

Study acronym: ICU
StatusCompleted
PhaseNot specified
Started
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Record History

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  1. Trial status changed: Unknown → Completed Show 8 more changesShow less
    • Final enrollment: 260 participants (planned 600)
    • Primary completion date changed from estimate of Dec 31, 2024 to Jan 6, 2025
    • Study completion date changed from estimate of Dec 31, 2024 to Jan 27, 2025
    • Start date: Jan 1, 2024 to Feb 1, 2023
    • Eligibility criteria expanded, about 15 words
    • Secondary endpoints: 1 to 3
    • Study description expanded, about 9 words
    • Site details revised
  2. Changed Registry marked status Unknown; last known: Recruiting
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This study collected data from patients with severe pneumonia to compare the duration of mechanical ventilation under different sedation regimens in real-world settings. It also evaluated and compared the sedation success rates, hemodynamic changes, and clinical outcomes of patients with severe pneumonia.
Trial Details
NCT Number NCT06514781
Lead Sponsor Xiangya Hospital of Central South University
Conditions
(from sponsor)		 Severe Pneumonia
Related terms Pneumonia
Enrollment 260 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov