Practice of Mechanical Ventilation in Patients With Severe Brain Injury in China
- Conditions
- Respiration, Artificial
- Registration Number
- NCT02517073
- Lead Sponsor
- Capital Medical University
- Brief Summary
The mechanical ventilation strategy has changed over years worldwide. Several international researches have been conducted to study the association of the use of mechanical ventilation with clinical outcomes. In this prospective, multicenter, cross-sectional survey, the practice of mechanical ventilation among patients with severe brain injury will be investigated in 70 intensive care units in China.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 104
- older than 18 years
- with severe brain injury (including severe traumatic brain injury, ischemic stroke, subarachnoid hemorrhage, spontaneous intracerebral hemorrhage, hypoxic-ischemic encephalopathy, intracranial tumor, intracranial infection and idiopathic epilepsy)
- mechanical ventilated for at least 24 hours before the time of on-spot survey
- undergoing a spontaneous breathing trial (SBT) at the time of on-spot survey
- underwent at least once SBT in the preceding 24 hours before time of on-spot survey
- enrolled in another trial
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Number of patients receiving control and assist mode of mechanical ventilation During 1 hour of on-spot survey Control mode is defined as volume or pressure control ventilation. Assist mode is defined as synchronized intermittent mandatory ventilation and pressure support ventilation.
- Secondary Outcome Measures
Name Time Method Duration of mechanical ventilation 60 days after on-spot survey Number of patients liberated from mechanical ventilation 60 days after on-spot survey The settings of tidal volume, inspiratory pressure, and positive end-expiratory pressure in enrolled patients During 1 hour of on-spot survey Neurological outcome by Glasgow Outcome Scale 60 days after on-spot survey
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (1)
ICU, Beijing Tiantan Hospital, Capital Medical University
🇨🇳Beijing, Beijing, China