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Power Lung Versus Acapella After Coronary Artery Bypass Graft Surgery

NCT05260944 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-04-21

No results posted yet for this study

Summary

The purpose of the study is to compare between the power lung versus acapella on airway clearance after coronary artery bypass graft surgery.

Conditions

  • Coronary Artery Bypass Graft Surgery

Interventions

DEVICE

Acapella device

patients will receive a two supervised sessions using acapella device three sets for 10 repetitions from the first day postoperative until 7 days, in addition to routine physiotherapy program (phase I cardiac rehabilitation, breathing exercises, postural drainage, percussion and vibration.

DEVICE

Power lung device

Group B. patients will receive a two supervised sessions using power lung device three sets for 10 repetitions from the first day postoperative until 7 days, in addition to routine physiotherapy program (phase I cardiac rehabilitation, breathing exercises, postural drainage, percussion and vibration.

OTHER

routine Physical Therapy program

Group C. Thirty patients will receive only routine physical Therapy program

Sponsors & Collaborators

  • South Valley University

    lead OTHER

Principal Investigators

  • Shymaa Y Abo zaid, Master · Assistant lecturer

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-05
Primary Completion
2023-07-05
Completion
2023-08-05

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05260944 on ClinicalTrials.gov