Respiratory Distress Syndrome of Newborn

2

Review clinical trials related to Respiratory Distress Syndrome of Newborn. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Surfactant Administration Methods in Preterm Infants With RDS: A Swedish Cohort Study

The goal of this observational study is to evaluate different methods of surfactant administration in preterm infants with respiratory distress syndrome (RDS). Preterm infants often have immature lungs and a deficiency of surfactant, a substance that helps keep the lungs open and supports oxygen exchange.Surfactant can be delivered to the lungs using different techniques, including INSURE (brief intubation), LISA (via a thin catheter), SALSA (via a laryngeal mask airway), and traditional administration via endotracheal intubation followed by mechanical ventilation. The main question this study aims to answer is:Which method of surfactant administration is associated with better clinical outcomes in preterm infants with RDS?The study will prospectively collect clinical data on infants receiving surfactant as part of standard care, with long-term follow-up using data from the Swedish Neonatal Quality Register. The results are intended to be used to inform the design of a future randomized multicenter study.

Participants needed: 300
Trial details
Biological sex: AllType: ObservationalSponsor: Vastra Gotaland RegionUpdated: Apr 24, 2026Duration: 6 Years
Eligibility criteria

Patient has received surfactant by any administration method [+3]

Status: Recruiting

Clinical Pharmacology of Dexamethasone in Pregnant Women With Preterm Labor

This study through to the pregnant woman blood concentrations of dexamethasone therapy after research, explore the pharmacokinetic data of dexamethasone in pregnant women, Chinese pregnant women dexamethasone pharmacokinetic model, provide a reference for the clinical use of dexamethasone dose, through the biomarkers of dexamethasone to promote fetal lung maturity and other metabolomics, It provides the basis for the effectiveness and safety study of dexamethasone.

Participants needed: 288
Trial details
Age: 20-40Biological sex: FemaleType: ObservationalSponsor: Dongyang LiuUpdated: Jan 26, 2022Locations: 1
Eligibility criteria

Aged 20-40 (inclusive); [+6]

Ectopic pregnancy; [+11]