Effects of Acapella VS Chest Physiotherapy on Dyspnea, Pulmonary Functions and Air Way Clearance in Post-Operative CABG Patients
Base Line + ACEPELLA
+ Base Line + Manual Chest Physiotherapy
Pulmonary Atelectasis+8
+ Dyspnea
+ Infections
Treatment Study
Summary
Study start date: May 23, 2023
Actual date on which the first participant was enrolled.This study focuses on helping patients who have undergone coronary artery bypass grafting (CABG) surgery, which is a procedure to improve heart blood flow. After this surgery, patients often face breathing issues and lung complications like pneumonia. The study compares two different methods to aid recovery: using an Acapella device and traditional chest physiotherapy. These methods aim to improve lung function, ease breathing difficulties, and clear mucus from the airways. Understanding which method works better could enhance recovery and reduce complications for post-CABG patients. Participants in the study are divided into two groups. One group uses the Acapella device along with standard treatments such as aerosol therapy and exercises, while the other group receives the same standard treatments plus 20 minutes of chest physiotherapy. The study measures lung capacity and breathing strength, as well as the amount of mucus cleared from the lungs. Conducted over six months in Lahore, Pakistan, the study excludes individuals with chronic lung disease or those who smoke, as these factors could affect the results. The goal is to find the most effective way to support recovery and improve breathing in patients after CABG surgery.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 55 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location