Viewing Study NCT06611683



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06611683
Status: COMPLETED
Last Update Posted: None
First Post: 2024-09-22

Brief Title: Effect of Inspiratory Muscle Training on Ventilated Patients in an Intensive Care Unit
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of Inspiratory Muscle Training on Ventilated Patients in an Intensive Care Unit
Status: COMPLETED
Status Verified Date: 2024-09
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: None
Brief Summary: The goal of this clinical trial is to learn if inspiratory muscle training facilite the liberation of mechanical ventilation The main questions it aims to answer are

Does inspiratory muscle training facilitate weaning from mechanical ventilation and enhance muscle strength in critically ill subacute adult patients

The main questions it aims to answer are

Does pulmonary rehabilitation facilitate wwaning form mechanical patients Does the intervention improve respiratory muscle strength and respiratory patterns

Participants received

Inspriatory muscle training twice daily for three consecutive weeks or until the subject no longer required ventilator support
Detailed Description: Patients on mechanical ventilation often experience rapid diaphragm atrophy on the second day resulting in muscle fiber changes respiratory muscle weakness Clinical studies have explored enhancing diaphragm and respiratory muscle strength and endurance through inspiratory muscle expiratory muscle and combined respiratory muscle training This study was to determine if inspiratory muscle training significantly facilitates liberation from mechanical ventilation and improves muscle strength when compared to without IMT among subacute critically ill adult patients

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