Human Surfactant Treatment of Respiratory Distress Syndrome Bicenter Trial

NCT00000570 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL

Last updated 2013-12-13

No results posted yet for this study

Summary

To determine if surfactant administration at birth in infants at high risk for respiratory distress syndrome (RDS) modified the clinical course of the syndrome.

Conditions

  • Lung Diseases
  • Respiratory Distress Syndrome

Interventions

DRUG

pulmonary surfactant

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    lead NIH

Principal Investigators

  • Thurman Merritt · University of California, San Diego

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION

Eligibility

Max Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1986-01-31
Completion
1990-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00000570 on ClinicalTrials.gov