Viewing Study NCT06454305



Ignite Creation Date: 2024-06-16 @ 11:51 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06454305
Status: RECRUITING
Last Update Posted: 2024-06-12
First Post: 2024-06-06

Brief Title: Effects of ACBT and Blow Bottle Technique in Patients With Abdominal Surgeries Under General Anesthesia
Sponsor: Riphah International University
Organization: Riphah International University

Study Overview

Official Title: Comparative Effects of Active Cycle of Breathing Technique and Blow Bottle Technique to Prevent Post-operative Pulmonary Complications in Patients With Abdominal Surgeries Under General Anesthesia
Status: RECRUITING
Status Verified Date: 2024-06
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: A postoperative pulmonary complication PPC is the most common serious complication after Abdominal surgery under GA which lead to longer hospital stays and have deleterious outcomes on lung volumes mucociliary clearance accumulation of mucus saliva and cough reflex Chest physiotherapy for airway clearance which includes postural drainage chest percussion vibrations Along with these breathing exercises such ACBT and Blow bottle technique are recommended to clear secretion which aid in enhancing pulmonary function by effectively mobilizing and eliminating excess bronchial secretions

This study of randomized clinical trial will check the comparative effect of ACBT and Blow Bottle Technique in patients with abdominal surgeries under GA by taking a sample of 44 patients through non probability convenience sampling technique Subject of both gender will be included between the age of 30 to 50 years who will undergoes with elective abdominal surgeries under GA Cholecystectomy Hysterectomy Appendectomy Hemorrhoidectomy and Laparoscopic open Elective surgeries under spinal anesthesia emergency surgeries cardiothoracic surgeries and hemodynamically unstable subjects will be excluded 22 subjects will receive ACBT and other 22 subjects will receive Blow bottle technique for 20 minutes duration per session two sessions per day for a period of 5 days The status of airway clearance oxygen saturation and lungs volumes will be measured pre and post intervention on day 1 and at the end of 5th day by using BCSS Pulse oximeter and Spirometer
Detailed Description: None

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