Trial reportEuropean journal of pediatrics2026
Original research: surfactant administration using less invasive surfactant administration (LISA) versus enhanced intubate-surfactant-extubate (ENSURE) in preterm infants.
Trial report in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Surfactant administration in late preterm and term neonates: is LISA ready for routine use?European journal of pediatrics · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Surfactant replacement therapy improves outcomes in preterm neonates with respiratory distress syndrome (RDS). While the less invasive surfactant administration (LISA) technique offers advantages over intubate-surfactant-extubate (INSURE), the enhanced INSURE (ENSURE) technique has been proposed to address procedural limitations of INSURE. However, direct comparisons between LISA and ENSURE are limited. This study aimed to compare the effectiveness of LISA and ENSURE in reducing the need for mechanical ventilation within 72 h in preterm neonates with RDS. In this open-label, single-center randomized controlled trial conducted at a tertiary-care hospital in North India, 118 preterm neonates (gestational age 26-35 weeks) requiring surfactant therapy were randomized to receive either LISA or ENSURE. The primary outcome was the need for invasive mechanical ventilation within 72 h of surfactant administration. Secondary outcomes included duration of respiratory support, ventilator-free days, intraventricular hemorrhage (IVH), bronchopulmonary dysplasia (BPD), mortality, and other neonatal morbidities. Baseline characteristics, including gestational age (30.6 vs. 31.3 weeks), birth weight (1442 vs. 1537 g), use of antenatal steroids (91.5% vs. 94.9%), were comparable between the two groups. The need for invasive mechanical ventilation within 72 h was similar in the LISA and ENSURE groups (32.2% vs. 33.9%; relative risk 0.95, 95% CI 0.57-1.59; p = 0.845). The duration of respiratory support, incidence of BPD, and mortality was also comparable.
conclusionLISA did not reduce the need for invasive mechanical ventilation within 72 h, duration of respiratory support, or neonatal morbidities and mortality compared with ENSURE.
trial registrationClinical Trial Registry of India (CTRI/2023/07/055841). WHAT IS KNOWN: •LISA reduces mechanical ventilation and BPD compared with conventional INSURE by preserving spontaneous breathing and avoiding prolonged positive pressure ventilation. •However, consistent superiority over other surfactant delivery techniques has not been demonstrated, with outcomes influenced by technique, expertise, patient selection, and protocol variability. WHAT IS NEW: •ENSURE showed comparable effectiveness to LISA in reducing invasive mechanical ventilation within 72 h. •These findings underscore that a standardized, protocol-driven surfactant strategy may be as important as the choice of technique.
Indexed as
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.