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Prevention of Infection of the Respiratory Tract Through Application of Non-Invasive Methods of Secretion Suctioning

Study acronym: PIRAMIDES
StatusNot Yet Recruiting
PhasePhase 4
Started
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Record History

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  1. Minor Interventions: airway clearance (Device) to Ceftriaxone 2 grams daily (Drug), airway clearance (Device), subglottic secretion aspiration (Device)
    • Study description shortened, about 13 words
    • Site details revised
    • Collaborator revised
    v6
  2. Notable Phase: Not applicable to Phase 4v5 Show 9 more changesShow less
    • Primary completion date: Jun 30, 2026 to Dec 30, 2028
    • Start date: May 19, 2025 to Sep 15, 2026
    • Primary endpoints: 2 to 1
    • Study completion date: Dec 20, 2026 to Jun 30, 2029
    • Eligibility criteria expanded, about 116 words
    • Secondary endpoints: 3 to 10
    • Study description expanded, about 245 words
    • Site details revised
    • Collaborators expanded, about 5 words
  3. Notable Primary completion date: Aug 2024 to Jun 30, 2026
    • Start date: Jul 2024 to May 19, 2025
    • Study completion date: Dec 2024 to Dec 20, 2026
    • Site details revised
    v4
  4. Notable Start date: Apr 2024 to Jul 2024v3
  5. Notable Start date: Dec 2023 to Apr 2024
    • Primary completion date: Jun 2024 to Aug 2024
    • Study completion date: Oct 2024 to Dec 2024
    v2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Adults who are unconscious or severely ill and need a breathing tube connected to a ventilator are at high risk of developing a lung infection (pneumonia) within the first few days in the intensive care unit. This early pneumonia affects up to 30 to 50 % of certain high-risk patients, prolongs the time on the ventilator and in hospital, and increases the use of antibiotics. Two strategies are commonly used today to try to prevent this infection: a short, three-day course of an intravenous antibiotic, and removal of secretions from the airway with a sterile suction catheter. Both have limitations - antibiotics can favour the growth of resistant bacteria, and catheter suctioning is uncomfortable and may injure the airway. PIRÁMIDES is a small (60-patient) pilot study that compares the current practice with two non-invasive, mechanical alternatives for keeping the airway clear: a continuous low-pressure suction system built into a special breathing tube, and a device that produces a gentle, programmed "artificial cough" through the ventilator. Adult patients who are intubated for severe trauma, severe brain injury, stroke, resuscitated cardiac arrest or other causes of decreased consciousness are randomly assigned, in equal numbers, to one of the three approaches and followed for 14 days, with a final visit at day 90. The main goal is to find out which of the three strategies best prevents early pneumonia, and which provides the best overall result for patients when survival, severity of infection, need for additional antibiotics and side effects are considered together. To make these comparisons as fair as possible in an open-label study, an independent committee of doctors not involved in patient care reviews each suspected pneumonia case without knowing which strategy the patient received. The results will help design a larger trial to confirm which approach is safest and most effective for preventing early pneumonia in critically ill patients on a ventilator.
Trial Details
NCT Number NCT06113939
Lead Sponsor Hospital San Carlos, Madrid
Collaborators: SAMUR-Protección Civil, Madrid, Spain
Conditions
(from sponsor)
Intubation Complication, Stroke, Ischemic, Stroke Hemorrhagic, Head Trauma, Cardiac Arrest, Ventilator Associated Pneumonia, Airway Clearance Impairment
Related terms Craniocerebral Trauma, Heart Arrest, Hemorrhagic Stroke, Ischemic Stroke, Pneumonia, Ventilator-Associated
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov