Actively Recruiting

Age: 0Days - 1Day
All Genders
ID06803498

Delivery Room Intervention and Evaluation (DRIVE) Network for Newborn Resuscitation Data Collection and Analysis

Led by American Academy of Pediatrics · Updated on 2025-01-31

3000000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

A

American Academy of Pediatrics

Lead Sponsor

C

Children's Hospital of Philadelphia

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are gathering and analyzing data on newborn infants who receive important resuscitation treatments right after birth in hospitals across the United States. This study focuses on babies who need help such as CPAP, positive pressure ventilation, intubation, or CPR in the delivery room. The goal is to better understand care practices, improve training, and reduce differences in infant outcomes by comparing data from many diverse hospitals. The study involves collecting detailed information on infants who receive significant resuscitation interventions at birth. These include basic and advanced procedures used to help babies breathe and stabilize immediately after delivery. The data come from a network of hospitals that represent various regions and populations. This network supports quality improvement by sharing feedback with each hospital to enhance resuscitation methods. Participants will have data collected on their resuscitation care and immediate outcomes, including where they go right after the intervention. Researchers will also track mortality within 30 days of birth. The network collects and coordinates this information to help hospitals improve newborn care and support ongoing research. The study includes infants from birth up to one day old and does not involve any additional treatment or procedures beyond usual care.

CONDITIONS

Brief Title

Delivery Room Intervention and Evaluation Network

Who Can Participate

Age: 0Days - 1Day
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Inborn infant who received significant resuscitation intervention such as CPAP, PPV, intubation, or CPR at birth
Not Eligible

You will not qualify if you...

  • Infant who was not born alive

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 30 days after birth

Participants who receive significant resuscitation interventions at birth are observed and data are collected on their resuscitation and outcomes.

Data collected during hospital stay and up to 30 days after birth

Trial Site Locations

Total: 1 location

1

American Academy of Pediatrics

Itasca, Illinois, United States, 60143

Actively Recruiting

Loading map...

Research Team

B

Beth Goins

J

Jessica Weglarz, MBA

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Similar Trials

Reducing Disparities for Children in Rural Emergency Resusci...

Pediatric Emergency Medicine

Actively Recruiting

2 locations

An Observational Study to Evaluate the Impact of Pregnancy a...

Cystic Fibrosis (CF)

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here