Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06511583
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-10
Brief Title:
FBS-ASaP Fibrobronchoscopy in ASpiration Pneumonia in the Emergency Department
Sponsor:
None
Organization:
None
Study Overview
Official Title:
FBS-ASaP Fibrobronchoscopy in ASpiration Pneumonia in the Emergency Department
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
FBS-ASaP
Brief Summary:
Non-Profit Prospective Observational Pilot Study
The study will have an overall duration of 3 years with patient enrollment starting after ethical committee approval
In this study all patients with a diagnosis of aspiration pneumonia who require aspiration of secretions or ingesta in the Emergency Department will be considered A registry will be created with the patients39 data noting the type of procedure performed laryngotracheal aspiration with a probe or with fibrobronchoscopy
This observational registry pilot study aims to evaluate the utility and adverse events related to the use of aspiration via videobronchoscopy performed in the Emergency Department and to compare the clinical outcomes of patients undergoing bronchoscopy with those treated only with blind laryngotracheal aspiration using a probe
The study will have an overall duration of 3 years with patient enrollment starting after ethical committee approval
In this study all patients with a diagnosis of aspiration pneumonia who require aspiration of secretions or ingesta in the Emergency Department will be considered A registry will be created with the patients39 data noting the type of procedure performed laryngotracheal aspiration with a probe or with fibrobronchoscopy
This observational registry pilot study aims to evaluate the utility and adverse events related to the use of aspiration via videobronchoscopy performed in the Emergency Department and to compare the clinical outcomes of patients undergoing bronchoscopy with those treated only with blind laryngotracheal aspiration using a probe
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None