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Clinical Trial Summary

The objective of the study is to compare the total duration of respiratory support in term neonates (≥37weeks) with meconium aspiration syndrome, who are provided early(≤2hr) bolus surfactant therapy versus standard care.


Clinical Trial Description

Enrolled participants will be randomly assigned to one of two study groups: 1. early(≤2hr) bolus surfactant replacement therapy or 2. standard care Intervention group: The neonates enrolled in this group will receive early bolus surfactant replacement therapy within 2hr of life. Control group: The neonates enrolled in this group will receive standard care according to standard unit protocol ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06090981
Study type Interventional
Source Lady Hardinge Medical College
Contact Sushma Nangia, MD, DM
Phone +919810838181
Email drsnangia@gmail.com
Status Recruiting
Phase N/A
Start date March 12, 2022
Completion date March 12, 2024

See also
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