Ignite Creation Date:
2024-05-06 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 1:55 PM
Study NCT ID:
NCT04732143
Status:
TERMINATED
Last Update Posted:
2023-06-13
First Post:
2021-01-27
Brief Title:
Effect of Preoperative Incentive Spirometer on Postoperative Pulmonary Complications Following Lung Resection
Sponsor:
Milton S Hershey Medical Center
Organization:
Milton S Hershey Medical Center
Study Overview
Official Title:
The Effect of Preoperative Inspiratory Muscle Training Using Incentive Spirometer on Postoperative Pulmonary Complications Following Lung Resection
Status:
TERMINATED
Status Verified Date:
2023-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Lack of funding and clinical resources to continue
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The objective of this study is to demonstrate that inspiratory muscle training with daily use of an incentive spirometer for at least 14 days prior to lung surgery will reduce the risk of post-operative pulmonary complications
Detailed Description:
Postoperative pulmonary complications PPC are the most common adverse events following lung resection with a reported incidence of over 20-30 in some series The objective of this study is to demonstrate that inspiratory muscle training IMT with daily use of an incentive spirometer IS for at least 14 days prior to lung surgery will reduce the risk of PPCs compared to the usual care consisting of no formal preoperative IMT The hypothesis is that preoperative inspiratory spirometer breathing ISB is a feasible and cost-effective intervention that can significantly reduce PPCs after lung resection It is also hypothesized that patient compliance with the intervention will be high because of its simplicity convenience low cost and no potential for adverse effects
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