Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06631716
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-01
Brief Title:
To Assess the Effectiveness of Three Distinct Mechanical Assisted Sputum Evacuation Apparatuses in the Treatment of Patients With Mechanical Ventilation-induced Atelectasis
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Evaluation of the Effectiveness of Mechanically Assisted Sputum Excretion
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
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:
EOTEOMASE
Brief Summary:
Retention of airway secretions is a common clinical problem in patients with mechanical ventilation Effective removal of airway secretions requires a balance between the production and removal of airway secretions through the mucociliary transport system Effective removal of airway secretions is the basic measure to maintain airway patency and normal alveolar ventilation and oxygenation At present a variety of mechanical assisted expectoration devices have been used to remove airway secretions in critically ill patients including The MetaNeb SystemMetaNeb High Frequency Chest Wall OscillationHFCWO and Cycloid Vibration TherapyCVT However there is still a lack of sufficient evidence to evaluate the clinical efficacy of these three different mechanical assisted expectoration devices in airway management of patients with mechanical ventilation This study aims to observe the clinical efficacy of three different mechanical assisted sputum evacuation devices in airway management of patients with mechanical ventilation atelectasis and to provide a basis for optimizing the airway management scheme of patients with mechanical ventilation
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