Skip to content

Pilot Trial of Surfactant Therapy For Preterm Neonates 5-21 Days Old With Respiratory Decompensation

Pilot Trial of Surfactant Therapy For Preterm Neonates 5-21 Days Old With

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00165074
Enrollment
11
Registered
2005-09-14
Start date
2003-06-30
Completion date
2007-06-30
Last updated
2007-11-22

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

Conditions

Respiratory Distress Syndrome

Keywords

Prematurity, Lung Disease, Hyaline Membrane, Surfactant

Brief summary

The purpose of the study is to determine whether additional surfactant(Infasurf) doses at 7 to 10 days of life time will improve lung function in premature infants, allowing a decrease in required oxygen concentration and ventilator settings.

Detailed description

Pulmonary surfactant is required for normal lung function. Preliminary data from previous trials suggest that more than half of chronically ventilated premature infants, greater than 1 week of age, have at least one episode of surfactant dysfunction, as measured in vitro, associated with a low surfactant protein B content. We propose to enroll premature infants less than 1250 gm birthweight, between days 5 and 21 of life who are intubated, mechanically ventilated, with a respiratory decompensation, defined as a severity score (mean airway pressure x FIO2) rising from a baseline of \< 1.8 to \> 3.5, sustained for \> 24 hours. Infants will receive two doses of Infasurf surfactant, 12-24 hours apart, at the standard dose of 3 ml/kg. Primary outcome is the change in respiratory severity score at 72 hours post surfactant treatment compared to pre-treatment. Sample size is 31 infants, study duration is 3 years, and recruitment of study patients will occur at the Hospital of the University of Pennsylvania, and Women and Children's Hospital of Buffalo.

Interventions

DRUGInfasurf (drug)

Infasurf 3 cc/kg instilled via endotracheal tube q 12-24 hours x 2 doses

Sponsors

University of Pennsylvania
CollaboratorOTHER
Women & Children's Hospital of Buffalo
CollaboratorOTHER
Children's Hospital of Philadelphia
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Days to 10 Days
Healthy volunteers
No

Inclusion criteria

* Less than 1250 gm birthweight * Day 5-21 of life * Intubated and mechanically ventilated, with respiratory decompensation, defined as the majority of daily severity scores (calculated every 6 hr from average of respiratory settings over 3-4 hour period) rising from baseline \< 1.8, to \> 3.5, sustained for \>24hr. Note: Prior surfactant therapy at birth is neither an inclusion nor exclusion criterion.

Exclusion criteria

* Serious congenital malformations * Life expectancy \< 7 days from enrollment * Patent ductus arteriosus at time of decompensation * Pulmonary hemorrhage as cause of respiratory decompensation * Active air leak syndrome at time of decompensation * Postnatal steroid therapy for lung disease

Design outcomes

Primary

MeasureTime frame
We hypothesize that at least 25% of treated infants will have a 50% or greater reduction in respiratory severity score at 72 hours compared to pre-treat72 hours

Outcome results

None listed

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