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RECRUITING
NCT07514481
NA

LISA vs Endotracheal Surfactant in Preterm Neonates: A Lung Ultrasound Distribution Study

Sponsor: Hamad General Hospital

View on ClinicalTrials.gov

Summary

This prospective, non-randomized, unblinded pilot study evaluates and compares the intrapulmonary distribution of exogenous surfactant in preterm neonates when administered via Less Invasive Surfactant Administration (LISA) versus conventional endotracheal intubation (ETT). Lung ultrasound (LUS) will be utilized to assess the pioneer Surfactant Distribution Homogeneity Index (SDHI) to quantify the evenness and extent of surfactant-induced lung aeration. Secondary objectives include evaluating changes in LUS scores, short-term clinical respiratory outcomes, and feasibility parameters for guiding future larger-scale trials.

Official title: A Prospective Pilot Controlled Trial Comparing the Intrapulmonary Distribution of Exogenous Surfactant Between (LISA) and Conventional Endotracheal Intubation in Preterm Neonates With RDS Using Lung Ultrasound and the NOVEL Surfactant Distribution Homogeneity Index (SDHI)

Key Details

Gender

All

Age Range

24 Weeks - 42 Weeks

Study Type

INTERVENTIONAL

Enrollment

22

Start Date

2026-01-01

Completion Date

2026-07-30

Last Updated

2026-04-07

Healthy Volunteers

No

Interventions

PROCEDURE

surfactant administration by ETT

Administration of exogenous surfactant (Beractant, 100 mg/kg in 4 mL/kg) via an endotracheal tube following intubation, accompanied by brief mechanical ventilation and extubation if feasible.

PROCEDURE

surfactant administration by thin catheter

Administration of exogenous surfactant (Beractant, 100 mg/kg in 4 mL/kg) via a thin catheter while the infant is maintained on non-invasive respiratory support (CPAP or NIPPV).

Locations (1)

Women's Wellness and Research Center (WWRC), Hamad Medical Corporation

Doha, Qatar