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A prospective study to compare the efficacy of Volume controlled ventilation and Pressure controlled ventilation in preventing post operative complications in patients undergoing off pump coronary artery bypass grafting.

A Prospective Randomised study to compare the efficacy of volume controlled ventilation and pressure support ventilation in patients undergoing coronary artery bypass grafting off pump surgeries. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088917
Enrollment
100
Registered
2025-06-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: I229- Subsequent ST elevation (STEMI) myocardial infarction of unspecified site

Interventions

Intervention1: To compare the efficacy of volume control ventilation and pressure support ventilation by comparing the post operative pulmonary complications in patients undergoing coronary artery byp

Sponsors

Kiranmuthrajah
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. 18 years of age or older 2. Scheduled for elective cardiac surgery with general anesthesia, invasive mechanical ventilation, complete median sternotomy

Exclusion criteria

Exclusion criteria: 1. Patients were excluded in case of emergent or redo surgeries 2. Patients with history of COPD. 3. Patients with known pulmonary Hypertension 4. Patients with EF less than 40% in Echocardiography 5. Patients with significant history of smoking addiction 6. Body mass index more than 35 kg/ m2 7. Obstructive sleep apnea 8. Patient Refusal

Design outcomes

Primary

MeasureTime frame
Development of post-operative pulmonary complications: (Post-extubation respiratory failure, Bronchospasm, Severe trachea bronchial congestion, Respiratory acidosis, Suspected or confirmed pneumonia, Pleural effusion, Radiological atelectasis, acute respiratory distress syndrome, prolonged invasive ventilation associated with hypoxemia)Timepoint: 30minutes/60minutes/2hours/4hours/8hour/16hours/24hours/48hours/72hours—

Secondary

MeasureTime frame
Duration of ICU stayTimepoint: At baseline—

Countries

India

Contacts

Public ContactDr Ranjith B Karthekeyan

Sri Ramachandra Institute of Higher Education and Research

ranjithkarthekeyan@sriramachandra.edu.in9841136568

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026