Viewing Study NCT06493123



Ignite Creation Date: 2024-07-17 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06493123
Status: RECRUITING
Last Update Posted: 2024-07-09
First Post: 2024-05-08

Brief Title: Cardiopulmonary Rehabilitation In Heart Valve Surgery
Sponsor: Istanbul Saglik Bilimleri University
Organization: Istanbul Saglik Bilimleri University

Study Overview

Official Title: Postoperative Mobilization and Bottle-PEP in Heart Valve SurgeryA Prospective Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
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: The aim of this study was to investigate the effects of postoperative early mobilization and Bottle-PEP application on respiratory parameters and functional capacity in patients undergoing heart valve surgery
Detailed Description: After all patients were informed about the study and potential risks patients who gave informed consent will be evaluated preoperatively and 5-7 days after surgery by the same investigator Patients will be randomly divided into 3 groups Group I n20 control - conventional cardiopulmonary rehabilitation Group II n20 conventional cardiopulmonary rehabilitation and Bottle PEP application Group III n20 will be included in the study as conventional cardiopulmonary rehabilitation and early mobilization group The respiratory parameters of the patients will be determined by a pulmonary function test and their functional capacities will be determined by a 6-minute walk test The preoperative and postoperative periods will be compared with statistical methods in the light of these evaluations on days 5-7

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