Surfactant Therapy Via Supraglottic Airway to Preterm Neonates With RDS in Vietnam

NCT ID: NCT07098910

Last Updated: 2025-09-22

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 440 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-25
• Study Completion Date: 2029-03-30

Brief 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.

Detailed Description

BACKGROUND

Respiratory distress syndrome (RDS) remains a leading cause of morbidity and mortality among preterm infants worldwide. Surfactant replacement therapy has significantly improved outcomes; however, standard techniques such as INSURE (Intubation-Surfactant-Extubation), while effective in avoiding mechanical ventilation, require endotracheal intubation-a procedure associated with potential complications and demanding considerable clinical expertise. Less invasive methods, such as surfactant administration via a laryngeal mask airway (SALSA), have shown promising results in reducing the need for mechanical ventilation in moderately preterm infants in smaller studies. This approach may be particularly beneficial in low- and middle-income countries (LMICs), where high birth volumes and limited availability of skilled personnel and advanced respiratory support highlight the need for simpler, safer interventions.

Evidence for SALSA in more immature preterm populations and from large randomized controlled trials remains limited. One key barrier to broader adoption has been the lack of appropriately sized supraglottic airway devices for very small infants. A recent feasibility study by this research team, using newly available preterm-sized devices, demonstrated that SALSA is feasible for surfactant delivery in infants weighing between 750 and 1500 grams (NCT06606444). A randomized controlled trial is now warranted to assess the effectiveness and safety of SALSA, particularly in lower-middle-income settings and among extremely low birth weight infants.

AIM AND HYPOTHESIS

This trial primarily aims to evaluate whether surfactant administration via the SALSA method is non-inferior to the current standard INSURE method in preventing IMV in preterm neonates with RDS admitted to a tertiary-level neonatal unit in South-Easia. It also seeks to compare the two methods in terms of safety, ease of use, infant comfort during the procedure, and morbidity during hospital admission.

We hypothesize that in preterm neonates with RDS, born before gestational week 34 and with a birth weight of at least 750 grams (P), surfactant administration via SALSA (I) will be non-inferior to INSURE (C) in preventing invasive mechanical ventilation (IMV) (O) within 72 hours after the procedure (T).

TRIAL DESIGN

This is an investigator-initiated, single-centre, two-arm parallel-group, open-label, non-inferiority RCT with a 1:1 allocation ratio per neonate. The trial entails an internal pilot-phase of the first 100 patients.

PARTICIPANTS:

See Eligibility section.

STUDY SITE

Phu San Hanoi Hospital (PSH) is the largest obstetric hospital in Hanoi, Vietnam, with about 40 000 deliveries every year and about 10% preterm births. The neonatal department is divided into three units: a level III NICU (35 beds), a high dependency unit (60 beds), and a Kangaroo mother care (KMC) unit (45 beds) which are staffed by 73 nurses and 21 doctors. Head ultrasound is made within 7 days of life and before discharge for all preterm infants <32 weeks of gestation as routine care, with additional assessments in between as needed. Echocardiography to screen for persistent ductus arteriosus is performed in neonates with clinical signs and treated medically (ibuprofen or paracetamol) if found haemodynamically significant. All infants <32 weeks of gestation are routinely examined for retinopathy of prematurity by ophthalmologist.

STUDY PROCEDURE

All infants requiring surfactant therapy will be screened for eligibility by the NICU team on a continuous basis. Caregivers will be approached for informed consent prior to inclusion. Eligible infants with consent will be randomized immediately before surfactant administration using a computer-generated, block-randomized sequence to receive either SALSA (intervention) or INSURE (control). The interventions are described in detail under "Arms and Interventions." For SALSA, a CE-marked, supraglottic airway device, Neo i-gel®, available in three sizes 0.85, 0.75, and 0.65 (Intersurgical Ltd), will be used. Procedural data will be collected through direct observation by the clinical team, while background characteristics and follow-up variables will be extracted from medical records by the study team. All data will be entered into an electronic case report form (eCRF) in REDCap. A subset of 50 patients per treatment arm will be video-recorded and reviewed for detailed analysis of procedure duration, physiologic stability and pain.

OUTCOMES

The primary outcome is: Failure of surfactant therapy to prevent invasive mechanical ventilation within 72 hours after first surfactant administration.

Decision to initiate mechanical ventilation via intubation will be made at the discretion of the treating physician, guided by the local NICU criteria for mechanical ventilation.

Secondary outcomes are listed under Outcome Measures.

SAMPLE SIZE

According to a baseline study conducted in 2023 (unpublished data), we assume that 21,5% of neonates in the control group (INSURE) would meet failure criteria. If there is no difference between SALSA and INSURE in terms of use of IMV (21,5% in both arms), 418 neonates need to be enrolled to be 80% sure that the upper limit of a one-sided 95% confidence interval will exclude an absolute difference larger than 10% in favour of INSURE. The sample is increased to 440 neonates to take into account a dropout of 5%.

PILOT PHASE

The trial will begin with an internal pilot phase designed to assess the feasibility of recruitment, adherence to trial procedures, data completeness, and intervention fidelity. Efficacy will not be evaluated. The internal pilot phase will enrol 100 neonates (approximately 23% of the total sample size), with recruitment anticipated over 12 months. This design will allow feedback on recruitment capacity and process quality and enabling adaptations.

The pilot phase will assess outcomes related to recruitment feasibility, adherence to intervention, adherence to mechanical ventilation criteria, retention, data completeness, data integrity and acceptability. Pilot outcomes are listed under Outcome Measures.

An interim assessment will be performed after the enrolment of 50 participants or after 12 months, whichever comes first. Only pilot outcomes will be assessed. The final analysis of the pilot phase will take place upon completion of enrolment of 100 participants. Following this evaluation, the Trial Steering Committee will determine whether to continue the study without modifications, implement protocol amendments-such as the inclusion of additional trial sites or adjustments to trial procedures-or temporarily suspend the trial to allow for a redesign. These decisions will be guided by a balanced assessment across all pilot domains.

Conditions

Respiratory Distress Syndrome in Premature Infant

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Surfactant therapy administered via supraglottic airway device (SALSA)

Study participants will receive surfactant therapy via a preterm size supraglottic airway device (SALSA).

Group Type: EXPERIMENTAL

Surfactant Administration Through Laryngeal or Supraglottic Airways (SALSA)

Intervention Type: PROCEDURE

While the infant is spontaneously breathing on nasal CPAP, the NICU physician will place the supraglottic airway device (SAD) and assess airway adequacy via CO₂ detection, chest movement, bilateral breath sounds, gastric insufflation, oxygen saturation, and heart rate. Each placement attempt should last no more than 30 seconds, with up to two attempts allowed. Surfactant (Curosurf 200 mg/kg) will be given slowly in 1-2 ml aliquots via a CE-marked preterm-sized SAD, Neo i-gel® (sizes 0.85, 0.75, 0.65; Intersurgical Ltd). The infant should primarily breathe spontaneously with PEEP from a T-piece resuscitator and receive gentle PPV if needed. PPV is continued for 30 seconds after surfactant administration before SAD removal. A reservoir bag may be used secondarily to provide PPV. If surfactant delivery via SALSA fails, the INSURE method (Intubation-Surfactant-Extubation) will be attempted.

Endotracheal intubation - surfactant administration - and extubation (INSURE)

Study participants will receive surfactant therapy administered via brief endotracheal intubation - surfactant administration - and extubation (INSURE).

Group Type: ACTIVE_COMPARATOR

Intubation - Surfactant administration - Extubation (INSURE)

Intervention Type: PROCEDURE

Study participants will receive surfactant therapy administered via brief endotracheal intubation - surfactant administration - and extubation (INSURE). Infants will be ventilated using a T-piece resuscitator with PEEP of 6 cm H20 and positive pressure ventilation (20 cm H20) for a couple of minutes (no more than 15 minutes) with adjustable FiO2. No mechanical ventilation will be used. Secondarily a reservoir-bag will be used for ventilation.

Interventions

Surfactant Administration Through Laryngeal or Supraglottic Airways (SALSA)

While the infant is spontaneously breathing on nasal CPAP, the NICU physician will place the supraglottic airway device (SAD) and assess airway adequacy via CO₂ detection, chest movement, bilateral breath sounds, gastric insufflation, oxygen saturation, and heart rate. Each placement attempt should last no more than 30 seconds, with up to two attempts allowed. Surfactant (Curosurf 200 mg/kg) will be given slowly in 1-2 ml aliquots via a CE-marked preterm-sized SAD, Neo i-gel® (sizes 0.85, 0.75, 0.65; Intersurgical Ltd). The infant should primarily breathe spontaneously with PEEP from a T-piece resuscitator and receive gentle PPV if needed. PPV is continued for 30 seconds after surfactant administration before SAD removal. A reservoir bag may be used secondarily to provide PPV. If surfactant delivery via SALSA fails, the INSURE method (Intubation-Surfactant-Extubation) will be attempted.

Intervention Type: PROCEDURE

Intubation - Surfactant administration - Extubation (INSURE)

Study participants will receive surfactant therapy administered via brief endotracheal intubation - surfactant administration - and extubation (INSURE). Infants will be ventilated using a T-piece resuscitator with PEEP of 6 cm H20 and positive pressure ventilation (20 cm H20) for a couple of minutes (no more than 15 minutes) with adjustable FiO2. No mechanical ventilation will be used. Secondarily a reservoir-bag will be used for ventilation.

Intervention Type: PROCEDURE

Other Intervention Names

Laryngeal mask airway surfactant administration; Surfactant Therapy via Laryngeal Mask Airway; Laryngeal Mask Airway for Surfactant Administration in Neonates; Supraglottic airway devices for surfactant treatment

Eligibility Criteria

Inclusion Criteria

• 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%

Exclusion Criteria

• Severe respiratory insufficiency in need of intubation at delivery room
• Severe respiratory insufficiency in need of intubation and invasive mechanical ventilation after arrival to NICU
• Previous surfactant administration
• Previous invasive mechanical ventilation
• Known pneumothorax
• Major malformations
• Physician not confident with study intervention
• The physician decided not to include the patient due to a preference for performing INSURE
• Excluded due to time constraints preventing completion of informed consent and trial procedures

• Maximum Eligible Age: 48 Hours
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Göteborg University

OTHER

Sponsor Role: collaborator

University of Padova

OTHER

Sponsor Role: collaborator

Hanoi Obstetrics and Gynecology Hospital

OTHER

Sponsor Role: collaborator

Karolinska Institutet

OTHER

Sponsor Role: lead

Responsible Party

Tobias Alfvén

Professor of Global Child Health

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Tobias Alfvén, Professor, M.D, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Department of Global Public Health, Karolinska Institutet, Solna, Sweden

Locations

Phu San Hanoi Hospital - Hanoi Obstetrics and Gynecology Hospital

Hanoi, , Vietnam

Site Status: RECRUITING

Countries

Vietnam

Central Contacts

Tobias Alfvén, Professor, M.D, Ph.D

Role: CONTACT

tobias.alfven@ki.se

+46 70 757 80 93

Mårten Larsson, M.D

Role: CONTACT

marten.larsson.2@gu.se

+46 704 24 09 72

Facility Contacts

Hien Vu, M.D.

Role: primary

hien.vu@ki.se

+84 904 999 455

References

Zapata HA, Fort P, Roberts KD, Kaluarachchi DC, Guthrie SO. Surfactant Administration Through Laryngeal or Supraglottic Airways (SALSA): A Viable Method for Low-Income and Middle-Income Countries. Front Pediatr. 2022 Mar 16;10:853831. doi: 10.3389/fped.2022.853831. eCollection 2022.

Reference Type: BACKGROUND

PMID: 35372140 (View on PubMed)

Dempsey T, Brismar TB, Svensson-Marcial A, Blennow M, Alfven T, Hook SM, Pejovic N. Radiologic evaluation of three smaller-sized supraglottic airway device prototypes for low-birth-weight neonates. Br J Anaesth. 2025 Nov;135(5):1551-1553. doi: 10.1016/j.bja.2025.05.038. Epub 2025 Jul 3. No abstract available.

Reference Type: BACKGROUND

PMID: 40610284 (View on PubMed)

Abdel-Latif ME, Walker E, Osborn DA. Laryngeal mask airway surfactant administration for prevention of morbidity and mortality in preterm infants with or at risk of respiratory distress syndrome. Cochrane Database Syst Rev. 2024 Jan 25;1(1):CD008309. doi: 10.1002/14651858.CD008309.pub3.

Reference Type: BACKGROUND

PMID: 38270182 (View on PubMed)

Related Links

https://www.clinicaltrials.gov/study/NCT06606444?cond=NCT06606444&rank=1

Feasibility study of SALSA using the same device at the same hospital in infants with birth weigh 750-1500g

Other Identifiers

Project-ID 2018-02770 VR

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

RS2020-0

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

ALFGBG-998065

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

2-4435/2024

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

2089 CN/PS

Identifier Type: -

Identifier Source: org_study_id