Clinical Trial:

Pediatric Respiratory Distress (PRO00003307)

Full Name

Prospective Observational Study of Respiratory Support Provided to Premature Infants at Risk for Respiratory Distress Syndrome

Description

If you agree to participate, after you sign the consent form, hospital records will be reviewed and reported during the first 7 days of life for your baby. Available health records regarding your pregnancy and delivery will also be reviewed. Health information that will be reported about you will only include information about your pregnancy and delivery such as the types of medication you received, medical conditions you may have had during your pregnancy, and how your baby was delivered. Health information that will be reported about your baby will only include information about your baby’s general health, diagnoses, medications, breathing conditions and care given during the first 7 days of life. No tests will be performed on you or your baby and you will not be asked to provide any information from a survey or questionnaires.

Eligibility

Inclusion Criteria
  • Infants ages 26 through 34 completed weeks (34 weeks, 6 days) postmenstrual age (PMA) who are at risk for respiratory distress syndrome
Doctor(s) Running This Study

Specialties

  • Neonatology

Affiliated with

LVPG Cliniciani