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Completed Phase 3 Interventional Results available

Comparison of Aerosol Delivery of Infasurf to Usual Care in Spontaneously Breathing RDS Patients

ClinicalTrials.gov ID: NCT03058666

Public ClinicalTrials.gov record NCT03058666. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 6:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Study to test the hypothesis that aerosolized Infasurf can decrease the need for intubation and instillation of liquid surfactant to the airway.

Study identification

NCT ID
NCT03058666
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ONY
Industry
Enrollment
477 participants

Conditions and interventions

Interventions

Drug · Device

Eligibility (public fields only)

Age range
1 Hour to 24 Hours
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 28, 2017
Primary completion
May 31, 2018
Completion
Jul 30, 2018
Last update posted
May 28, 2024

2017 – 2018

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
USA Children's & Women's Hospital Mobile Alabama 36604
Banner - University Medical Center Phoenix Phoenix Arizona 85006
Sharp Mary Birch Hospital for Women & Newborns San Diego California 92123
Baptist Hospital of Miami Miami Florida 33176
Adventist Healthcare System, Florida Hospital Orlando Florida 32803
Johns Hopkins All Children's Hospital St. Petersburg Florida 33701
University of South Florida, Tampa general Tampa Florida 33606
Columbus Regional Hospital Columbus Georgia 31904
OSF Saint Francis Medical Center Peoria Illinois 61637
Kentucky Children's Hospital, University of Kentucky Medical Center Lexington Kentucky 40506
Children's Hospital and Clinics Minneapolis Minnesota 55404
Children's Hospital Minnesota Saint Paul Minnesota 55102
University of Mississippi Medical Center Jackson Mississippi 39216
Sisters of Charity Hospital Buffalo New York 14214
Pitt County Memorial Hospital Greenville North Carolina 27835
The Medical University of South Carolina Charleston South Carolina 29425
Jackson-Madison County General Hospital Jackson Tennessee 38301
Vanderbilt university Medical Center Nashville Tennessee 37232
North central Baptist Hospital San Antonio Texas 78258
Timpanogos Regional Medical Center Orem Utah 84057
Utah Valley Hospital Provo Utah 84604
University of Virgina Medical Center Charlottesville Virginia 22903

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03058666, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 28, 2024 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03058666 live on ClinicalTrials.gov.

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