Viewing Study NCT02478411



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Last Modification Date: 2024-10-26 @ 11:45 AM
Study NCT ID: NCT02478411
Status: UNKNOWN
Last Update Posted: 2019-08-08
First Post: 2015-06-14

Brief Title: Early Cycloergometric Physiotherapy in Critically Ill Patients With Invasive Mechanical Ventilation
Sponsor: Hospital Son Llatzer
Organization: Hospital Son Llatzer

Study Overview

Official Title: Functional and Motor Effects of an Early Cycloergometric Physiotherapy Program in Critically Ill Patients With Invasive Mechanical Ventilation A Randomized Controlled Trial
Status: UNKNOWN
Status Verified Date: 2019-08
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Study designed to evaluate the functional and motor effects in critically ill subjects at ICU and hospital discharge with the incorporation of a mobilization program of cycloergometric physiotherapy sessions compared with conventional physiotherapy
Detailed Description: Cycloergometric treatment is described to improve the functional and motor status of critically ill subjects However there are few studies comparing cycloergometric physiotherapy and conventional physiotherapy in intensive care subjects under mechanical ventilation The most relevant of these studies conducted by Burtin et al showed beneficial effects of cycloergometric treatment However the duration of the physiotherapy sessions in this study differed between groups as cycloergometric group received a double daily dose of treatment It is known that the intensity of physiotherapy also affects the functional and motor status

For this reason the investigators designed a randomized controlled study with early cycloergometric or conventional treatment with the same intensity between groups to analyze objective functional and motor endpoints

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