Noninvasive Support Methods for Acute Respiratory Failure of Community-acquired Pneumonia
Recruiting now · Not applicable
Conditions studied: Community-acquired Pneumonia, Community-Acquired Infections
In brief
This randomized controlled trial aims to compare the efficacy and safety of high-velocity nasal insufflation (HVNI) versus standard noninvasive ventilation (NIV) in adult patients experiencing acute exacerbations of community-acquired pneumonia (CAP) accompanied by hypoxemic respiratory failure. The primary focus is on assessing treatment failure within 48 hours, defined as the need for intubation or death. Secondary outcomes include evaluations of gas exchange parameters, patient comfort levels, duration of ICU stay, and 28-day mortality rates.
Key facts
- Study ID
- NCT06996834
- Run by
- Assiut University
- People needed
- 100
- Starts
- 2025-07-01
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2026-04-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years
- Clinical and radiographic diagnosis of CAP
- Respiratory failure using partial pressure of oxygen (PaO₂) and fraction of inspired oxygen (FiO₂) is defined by a partial pressure of oxygen/fraction of inspired oxygen ratio (PaO₂/FiO₂) ≤ 300 mmHg or a respiratory rate (RR) ≥ 25/min
- Informed consent obtained
You may not qualify if…
- Hemodynamic instability requiring vasopressors
- Altered mental status Glasgow Coma Scale (GCS < 13)
- Contraindication to NIV or HVNI (facial trauma, recent upper airway surgery)
- Do-Not-Intubate (DNI) order
Where it is running
- Assuit University — Asyut, Assuit, Egypt (enrolling)
Full record on ClinicalTrials.gov
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