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Non Inferiority Trial Investigating Surfactants Administered Via MIST

Non Inferiority Trial Investigating Surfactants Administered Via MIST

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06074380
Acronym
Niftisurf
Enrollment
262
Registered
2023-10-10
Start date
2024-01-01
Completion date
2027-12-01
Last updated
2025-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Distress Syndrome

Keywords

Pulmonary Surfactant, CPAP, Neonate

Brief summary

RESEARCH DESIGN Multicenter, randomized, controlled trial. RECRUITMENT Entry criteria Preterm infants 28-35 6/7 weeks' gestation and less than 48 hours of age who have a clinical diagnosis of respiratory distress syndrome. Infants who are on NCPAP and FiO2 ≥0.30 will randomized to curosurf or infasurf via MIST. Exclusion criteria Infants will be excluded if there is a congenital anomaly or an alternative cause for respiratory distress. Babies who require emergent intubation will not be enrolled in the interventions. Parental Consent will be obtained prior to randomization.

Detailed description

INTERVENTION Infants who on CPAP who reach the threshold of 30% oxygen will be randomized to calfactant (Infasurf), 3ml/kg or poractant alfa (Curosurf), 2.5ml/kg, administered under direct laryngoscopy using a surfactant instillation catheter (MIST) 16G Angiocath (Becton Dickinson, Sandy, UT, USA). A second dose of calfactant (Infasurf) 3ml/kg or poractant alfa (Curosurf), 1.25ml/kg, will be administered via MIST their fiO2 reaches the threshold of 30% between 6 and 48 hours after the first dose. No further surfactant should be given in the first 7 days unless the infant reaches the intubation criteria. POST-INTERVENTION MANAGEMENT Other than the requirement to adhere to intubation criteria in the first week, and in some cases perform a room air trial at 36 weeks corrected gestation, management will be at the discretion of the clinical team. Titration of CPAP pressure is encouraged, with a permitted maximum of 8 cm H2O. Use of nasal IPPV is allowable for apnea, but discouraged for RDS and should only be after at least one dose of surfactant has been given. Early caffeine therapy is expected. Criteria for intubation: Enrolled infants on CPAP will be intubated if: * FiO2 ≥0.45 for 15 minutes, or if there is unremitting apnea (\> 6 episodes/hour requiring intervention or in the opinion of the treating physician) or persistent respiratory acidosis (pH\<7.25 and pCO2 \>60) on blood gasses at least 30 minutes apart or metabolic acidosis refractory to treatment. * Need for an anesthetic or an intervention requiring intubation These criteria apply during the first week of life, and to the first episode of intubation only. If the infant is intubated it is expected that another dose of surfactant will be administered.

Interventions

DRUGMIST surfactant

Surfactant will be given via MIST while neonate is on CPAP

Sponsors

Endeavor Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

Surfactant will be sent from Investigational Pharmacy

Intervention model description

Comparison of the efficacy of calfactant compared to poractant alfa administered with a minimally invasive method for the treatment of respiratory distress syndrome in 28-36 week infants

Eligibility

Sex/Gender
ALL
Age
No minimum to 48 Hours
Healthy volunteers
No

Inclusion criteria

* Preterm infants 28-35 6/7 weeks' gestation and less than 48 hours of age who have a clinical diagnosis of respiratory distress syndrome confirmed by a chest x-ray on nasal continuous positive airway pressure (NCPAP) and FiO2 ≥0.30

Exclusion criteria

* Infants will be excluded if there is a congenital anomaly or an alternative cause for respiratory distress. * Infants who require emergent intubation will not be enrolled in the interventions.

Design outcomes

Primary

MeasureTime frameDescription
Number of infants requiring Endotracheal Intubation7 daysInfants will have an endotracheal placed if their inspired oxygen is \>45% for more than 15 minutes

Secondary

MeasureTime frameDescription
Duration of positive pressure support36 weeks corrected gestational ageEndotracheal ventilation or Non-invasive Ventilation or CPAP or NC flow\>2 L
Duration of Supplemental oxygen36 weeks corrected gestational ageOxygen requirement to keep saturations \>95%

Countries

United States

Contacts

Primary ContactMatthew Derrick
mderrick@northshore.org18475702920

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026