LISA vs Endotracheal Surfactant in Preterm Neonates: A Lung Ultrasound Distribution Study
Recruiting now · Not applicable
Conditions studied: Respiratory Distress Syndrome, Newborn
In brief
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.
Key facts
- Study ID
- NCT07514481
- Run by
- Hamad General Hospital
- People needed
- 22
- Starts
- 2026-01-01
- Expected to finish
- 2026-07-30
- Last updated by the study team
- 2026-04-07
Who can join
Age: 0 and older, up to 1. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Gestational age 24+0 to 42+6 weeks. Clinical and radiographic diagnosis of Respiratory Distress Syndrome (RDS). Requirement for surfactant within the first 3 days of life. Written informed parental consent.
You may not qualify if…
- Infants intubated at birth or who received surfactant prophylactically in the delivery room.
- Major congenital anomalies or lung malformations (e.g., congenital diaphragmatic hernia, pulmonary hypoplasia).
- Syndromic or genetic conditions affecting lung or chest wall development. Severe hemodynamic instability or congenital heart disease requiring intensive support.
- Lack of parental consent for trial participation.
Where it is running
- Women's Wellness and Research Center (WWRC), Hamad Medical Corporation — Doha, Qatar (enrolling)
Full record on ClinicalTrials.gov
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