Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Inborn infant who received significant resuscitation intervention such as CPAP, PPV, intubation, or CPR at birth
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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