Ignite Creation Date:
2024-05-06 @ 8:08 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06264856
Status:
SUSPENDED
Last Update Posted:
2024-02-20
First Post:
2023-04-03
Brief Title:
Bronchoscopy for Thoracic Trauma Patients
Sponsor:
National Taiwan University Hospital
Organization:
National Taiwan University Hospital
Study Overview
Official Title:
Flexible-bronchoscopy Trial for Moderate and Severe Thoracic Trauma Patients Without Brain Injury
Status:
SUSPENDED
Status Verified Date:
2023-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
The principal investigator will be studying abroad for one year The study is expected to resume enrollment from December 1 2024
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The study aims to evaluate the effectiveness of bronchoscopic sputum suction in patients with severe thoracic illness-induced respiratory failure The study will compare the outcomes of patients who receive bronchoscopic sputum suction versus blind negative pressure aspiration for sputum removal The study will measure baseline data postoperative blood gas conditions and clinical parameters such as time of invasive ventilation total time of ventilation hospital stay weaning success rate reintubation rate ventilator-associated pneumonia incidence and fatality rate The study aims to determine whether bronchoscopy-assisted sputum removal is superior to blind negative pressure aspiration in improving patient outcomes
Detailed Description:
The aim of the present randomized control trial is to assess the value of bronchoscopic sputum suction in patients with severe thoracic illness-induced respiratory failure To decrease group differences in baseline characteristics and blood gas conditions patients will be randomly assigned to receive either bronchoscopy-assisted or negative pressure aspiration for sputum suction while the remaining treatment course will be the same The study will measure major clinical indicators such as time of invasive ventilation total time of ventilation hospital stay weaning success rate reintubation rate ventilator-associated pneumonia incidence and fatality rate to provide strong evidence for the efficacy of each suction method
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None