Surfactant Therapy Via Supraglottic Airway Device Versus Endotracheal Intubation to Prevent Mechanical Ventilation in Preterm Neonates With Respiratory Distress Syndrome: An Open-label, Non-inferiority, Randomized Controlled Trial at a Level-III Neonatal Intensive Care Unit in Vietnam

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Preterm babies often have trouble breathing because their lungs are not fully developed. This condition is called respiratory distress syndrome (RDS). A medicine called surfactant helps their lungs open up and work better. It is usually given through a procedure called INSURE, where a breathing tube is placed into the baby's trachea (via an endotracheal tube) to deliver the medicine. While effective, this method is invasive and can be uncomfortable and risky for the baby. A newer, less invasive method called SALSA uses a soft mask placed in the throat (a laryngeal mask airway) instead of an endotracheal tube to give the surfactant. This randomized controlled trial will compare SALSA to the traditional INSURE method to see if it works just as well in preventing the need for invasive breathing support within three days of treatment. The study will include preterm babies born before 34 weeks of pregnancy and weighing at least 750 grams, at Phu San Hanoi Hospital in Vietnam. If SALSA is found to be safe and effective, it may offer a gentler, less invasive, and easier-to-perform option for treating respiratory distress syndrome in premature babies.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 2 days
Healthy Volunteers: f
View:

• Inborn neonate (=born in the hospital), AND

• Gestational age \<34+0 weeks, AND

• Birth weight ≥750g, AND

• Age \<48 hours, AND

• Diagnosis of RDS, confirmed with a chest x-ray or lung ultrasound, except in cases where immediate treatment is necessary and imaging would cause a delay AND

• Indication for surfactant treatment: Infant on non-invasive support (CPAP/NIPPV) and FiO2 \>0.30 to maintain oxygen saturation (SpO2) between 90% and 95%

Locations
Other Locations
Viet Nam
Phu San Hanoi Hospital - Hanoi Obstetrics and Gynecology Hospital
RECRUITING
Hanoi
Contact Information
Primary
Tobias Alfvén, Professor, M.D, Ph.D
tobias.alfven@ki.se
+46 70 757 80 93
Backup
Mårten Larsson, M.D
marten.larsson.2@gu.se
+46 704 24 09 72
Time Frame
Start Date: 2025-09-25
Estimated Completion Date: 2029-03-30
Participants
Target number of participants: 440
Treatments
Experimental: Surfactant therapy administered via supraglottic airway device (SALSA)
Study participants will receive surfactant therapy via a preterm size supraglottic airway device (SALSA).
Active_comparator: Endotracheal intubation - surfactant administration - and extubation (INSURE)
Study participants will receive surfactant therapy administered via brief endotracheal intubation - surfactant administration - and extubation (INSURE).
Related Therapeutic Areas
Sponsors
Collaborators: University of Padova, Göteborg University, Hanoi Obstetrics and Gynecology Hospital
Leads: Karolinska Institutet

This content was sourced from clinicaltrials.gov