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Comparison of mechanical power between Pressure Controlled ventilation versus Volume control ventilation in children undergoing laparoscopic surgery under general anesthesia A randomised controlled trial.

Comparison of mechanical power between PCV vs VCV in children undergoing laparoscopic surgery under general anesthesia. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093164
Enrollment
132
Registered
2025-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Pressure controlled ventilation: Positive End Expiratory Pressure,Tidal Volume,Inspiratory Pressure,Mechanical Power,Driving Pressure Control Intervention1: Volume controlled ventilatio

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)age between 1 years and 12 years 2)ASA status I to III 3)elective laparoscopic surgery with a duration exceeding 1 hour

Exclusion criteria

Exclusion criteria: 1)Parental refusal to participate 2) History of severe cardiac and neurological diseases 3) History of severe lung disease (Pneumothorax, Pulmonary TB, Pleural effusion ) 4) children with known deformities of chest wall or thoracic spine

Design outcomes

Primary

MeasureTime frame
calculation of mechanical power on volume control mode in group V and pressure control mode in group P, derived by measuring the following Respiratory mechanics parameters: Following parameters will be measured Driving pressure ,Peak airway pressure Mean airway pressure, Plateau pressure Static Lung compliance Timepoint: after induction of anesthesia, before pneumoperitoneum,15 minutes after pneumoperitoneum,just after deflation of pneumoperitoneum

Secondary

MeasureTime frame
1)Blood pressure- systolic blood pressure & Diastolic blood pressure 2)oxygen saturation (spo2)Timepoint: Every 15 minutes during the trial

Countries

India

Contacts

Public ContactDadi Bote Nonang

All India Institute of Medical Science

Pateldrnishant@gmail.com8510955882

Outcome results

None listed

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