Completed

Effects of Acapella VS Chest Physiotherapy on Dyspnea, Pulmonary Functions and Air Way Clearance in Post-Operative CABG Patients

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Base Line + ACEPELLA

+ Base Line + Manual Chest Physiotherapy

Other
Who is being recruted

Pulmonary Atelectasis+8

+ Dyspnea

+ Infections

From 55 to 70 Years
+13 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: May 2023
See protocol details

Summary

Principal SponsorRiphah International University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleEffects of Acapella VS Chest Physiotherapy on Dyspnea, Pulmonary Functions and Air Way Clearance in Post-Operative CABG Patients
NCT06317363
Principal SponsorRiphah International University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Pulmonary AtelectasisDyspneaInfectionsLung DiseasesPneumoniaRespiration DisordersRespiratory Tract DiseasesRespiratory Tract InfectionsSigns and SymptomsSigns and Symptoms, RespiratoryPathological Conditions, Signs and Symptoms

Criteria

5 inclusion criteria required to participate
both gender

Patients aged between 55-70 years

Vitally Stable

extubated post-CABG day 01 patients

Show More Criteria

8 exclusion criteria prevent from participating
With a history of chronic obstructive pulmonary disease or asthma patient

Intubated patient

Surgical complication after CABG

With a history of smoking

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Group A (baseline treatment + acapella)

Group II

Experimental
Group B (baseline + manual chest physiotherapy)

Study 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

Suspended

Jinnah Hospital

Lahore, PakistanOpen Jinnah Hospital in Google Maps
CompletedOne Study Center