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Recruiting Not applicable

Comparing Different Startegies of Positive Pressure Ventilation in Children

NCT06612125 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2024-10-01
Last updated
2025-01-09

Condition(s) studied

Ventilation Therapy; Complications

Investigational drug(s) / intervention(s)

volume controlled ventilationpressure controlled ventilationpressure controlled volume grantanteed ventilation

volume controlled ventilation: Pediatric patients in the VCV group (n= 30) received volume-controlled ventilation, target tidal volume was set at 7 mL/kg, with a respiratory rate of 16 breaths/min and a respiratory ratio of 1:2.

pressure controlled ventilation: Pediatric patients in the PCV group(n=30) received pressure-controlled ventilation. The initial parameters will be as follows: the peak inspiratory pressure (PIP) will set to provide a tidal volume of 7 ml/kg , respiratory rate will be 16 breaths/min, inspiratory to expiratory ratio was 1:2 with an upper limit of PIP of 20 cm H2O.

pressure controlled volume grantanteed ventilation: Pediatric patients in the PCV-VG group (n=30)will be conducted with pressure-controlled volume-guaranteed ventilation, target tidal volume will set at 7 mL/kg, with a respiratory rate of 16 breaths/min and a respiratory ratio of 1:2.

Study summary

The most basic modes of mechanical ventilation are volume-controlled ventilation (VCV) and pressure-controlled ventilation (PCV). VCV guarantees a target volume of ventilation using a constant flow, but may lead to high peak airway pressure (Ppeak) during the gas insufflation . In PCV mode, on the other hand,

Eligibility

Sex
ALL
Min age
1 Year
Max age
5 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. age between 1 and 5 years. 2. patient scheduled for laparoscopic inguinal hernia repair. 3. American Society of Anesthesiologists classification of physical status of I-II. Exclusion Criteria: 1. cardiopulmonary disease. 2. severe hepatorenal dysfunction. 3. history of upper respiratory tract infection 2 weeks before the operation. 4. overweight \[more than 20% of standard body weight\]. 5. neuromuscular disease. 6. anticipated difficult airway. 7. hiatus hernia or gastroesophageal reflux disease.

Primary outcome measure(s)

  • (PIP) — within one hour
    peak inspiratory pressure
  • Pplat — within one hour
    plateau airway pressure
  • (Cdyn) — within one hour
    pulmonary dynamic compliance
  • (RAW — within one hour
    airway resistance
  • VT — within one hour
    exhaled tidal volume
  • EtCO2 — within one hour
    end-expiratory carbon dioxide
  • Vd/VT — within one hour
    physiologic dead space over tidal volume

Trial sites (1)

FacilityCityRegionStatus
Benisuef university hospital Benisuef Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06612125 on ClinicalTrials.gov ↗ ← All trials in Egypt