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Clinical Trial Summary

This prospective randomized comparative study, to assess post-operative lung atelectasis by comparing calculated lung score using ultrasound between pediatric patients intubated with LMA (laryngeal mask airway) under volume versus pressure controlled modes of ventilation.


Clinical Trial Description

The initial US scanning will be done prior to the induction of anesthesia. Induction of anesthesia using 4% sevoflurane. Adequate size LMA will be inserted after adequate depth of anesthesia adjusted. Group A (n=25): will receive pressure-controlled ventilation (PCV). Group B (n=25): will receive volume-controlled ventilation (VCV). US scanning and Arterial blood gases at the following: - T1(After maintenance of anesthesia). - T2 (One minute after applying groin bandage and before extubation). - T3 (10 minutes after extubation and resumption of adequate regular breathing). - T4 (30 min post extubation). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06076395
Study type Interventional
Source Kasr El Aini Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date January 12, 2024
Completion date August 2024