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Practice of Mechanical Ventilation in Patients With Severe Brain Injury in China

Information source: Capital Medical University
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Respiration, Artificial

Phase: N/A

Status: Recruiting

Sponsored by: Capital Medical University

Official(s) and/or principal investigator(s):
Jian-Xin Zhou, MD, Study Chair, Affiliation: Acute Brain Injury and Critical Care Research Collaboration, ABC Research Collaboration

Overall contact:
Jian-Xin Zhou, MD, Phone: 8610 67096579, Email: zhoujx.cn@gmail.com

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.

Clinical Details

Official title: A Survey on the Practice of Mechanical Ventilation Among Patients With Severe Brain Injury in China: a Prospective Observational Study

Study design: Observational Model: Case-Only, Time Perspective: Cross-Sectional

Primary outcome: Number of patients receiving control and assist mode of mechanical ventilation

Secondary outcome:

The settings of tidal volume, inspiratory pressure, and positive end-expiratory pressure in enrolled patients

Duration of mechanical ventilation

Number of patients liberated from mechanical ventilation

Neurological outcome by Glasgow Outcome Scale

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria: 1. older than 18 years 2. 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) 3. mechanical ventilated for at least 24 hours before the time of on-spot survey Exclusion Criteria: 1. undergoing a spontaneous breathing trial (SBT) at the time of on-spot survey 2. underwent at least once SBT in the preceding 24 hours before time of on-spot survey 3. enrolled in another trial

Locations and Contacts

Jian-Xin Zhou, MD, Phone: 8610 67096579, Email: zhoujx.cn@gmail.com

ICU, Beijing Tiantan Hospital, Capital Medical University, Beijing, Beijing 100050, China; Recruiting
Jian-Xin Zhou, MD, Phone: 8610 67096579, Email: zhoujx.cn@gmail.com
Additional Information

Starting date: August 2015
Last updated: August 11, 2015

Page last updated: August 20, 2015

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