Skip to content

Preoperative incentive spirometry for preventing postoperative pulmonary complications in patients undergoing coronary artery bypass graft surgery: A prospective, randomized controlled trial

Preoperative incentive spirometry for preventing postoperative pulmonary complications in patients undergoing coronary artery bypass graft surgery: A prospective, randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20201020005
Enrollment
Unknown
Registered
2020-10-20
Start date
2019-06-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

postoperative pulmonary complications&#44

Interventions

2 days preoperative&#44
practices incentive spirometry prescribed and ABGs obtained. incentive spirometry was used every 4 hr for 10 min for each session ,used incentive spirometry every 4 hr for 10 min for each session pos
Experimental Device,No Intervention No treatment
incentive spirometry,Control group

Sponsors

Essa Sweity (MSc )
Lead Sponsor
Aidah alkaissi (PhD),Wafiq Othman (MD&#44
Collaborator
Anesthesiologist)
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. 18 years or older 2. Scheduled to have coronary artery bypass grafting (CABG) 3. Patients who were well motivated and compliant.

Exclusion criteria

Exclusion criteria: 1. Patients who are expected not to be able to conduct or comply with IS,such as patients with cognitive or neurological deficits 2. Patients with coexisting acute or chronic respiratory disorders 3. Patients unable to understand or show the proper use of the incentive spirometer 4. Patients who cannot be instructed or supervised to assure appropriate use of the device 5. Patients in whom cooperation is absent or patients unable to understand or demonstrate proper use of the device 6. Patients who are confused or delirious 7. Patients undergoing any other surgery along with CABG, having prolonged mechanical ventilation (more than 24 hours). 8. Patients undergoing emergency CABG surgery. 9. chronic obstructive pulmonary disease (COPD), asthma, restrictive lung disease 10. Preoperative major chest infection e.g. pulmonary tuberculosis, chest deformities such as pectus carinatum, pectus excavatum, thoracolumbar scoliosis, diaphragmatic hernias diagnosed on history.

Design outcomes

Primary

MeasureTime frame
Postoperative pulmonary complication (PPC) : Atelectasis daily for 3 day postoperatively chest X-ray,Postoperative pulmonary complication (PPC) : Plural effusion , pneumonia, pneumothorax daily for 3 day postoperatively chest X-ray

Secondary

MeasureTime frame
Oxygenation status / PaO2/FiO2 every 6 hour's postoperatively Arterial blood gases ,ICU length of stay Days Date Count,Hospital stay Days Date Count,Mechanical ventilation duration hours Date Count

Contacts

Public ContactEssa Sweity

An-Najah National University

essasweity@gmail.com+970 598428085

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026