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Optimal Timing for Spontaneous Breathing Trials

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 6 months later Jun 30, 2026 → Dec 30, 2026
See other at-risk trials from Rush University Medical Center

Record History

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  1. Primary completion pushed from Jun 30, 2026 to Dec 30, 2026 Show 5 more changesShow less
    • Study completion pushed from Dec 30, 2026 to Feb 28, 2027
    • Eligibility criteria expanded, about 7 words
    • Secondary endpoints: details revised at 2 of 5 entries
    • Site contact updated
    • Publications: details revised at 4 of 4 entries
  2. Primary completion date: Dec 31, 2025 to Jun 30, 2026
    • Study completion date: Jun 30, 2026 to Dec 30, 2026
    • Site contact updated
    v3
  3. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Sep 30, 2024 to Sep 17, 2024
    • Site details revised
    v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 aims to explore how the timing of Spontaneous Breathing Trials (SBTs) affects recovery in adult patients who are on mechanical ventilation in the ICU. SBTs are tests used to determine if a patient is ready to breathe on their own without the help of a ventilator. The study will compare two different timing strategies for these trials: one group of patients will have the test early in the morning, while the other group will have it later in the morning. By observing the outcomes, such as how long patients need to stay on the ventilator, the study hopes to find the best time to perform these trials to help patients recover more quickly and safely.
Trial Details
NCT Number NCT06561295
Lead Sponsor Rush University Medical Center
Conditions
(from sponsor)		 Respiration, Artificial, Weaning
Related terms Respiratory Aspiration
Enrollment 348 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov