Application to Predict Neonatal Apnea With Bradycardia

Starting soon · Not applicable · Has a placebo group

Conditions studied: Apnea Neonatal, Bradycardia Neonatal

In brief

This purpose of this study is to reduce or stop apneas and bradycardias in pre-term infants, before they occur using gentle stimulation.

Key facts

Study ID

NCT06852053

Run by

University of Alabama at Birmingham

People needed

25

Starts

2026-09-01

Expected to finish

2027-12-31

Last updated by the study team

2026-07-07

Who can join

Age: 0 and older, up to 1. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Documented episodes of apnea with bradycardia over the previous 24 hours.
• Off ventilatory support/NCPAP for > 48 hours prior to study entry
• Gestational age < 32 0/7 weeks' gestation at birth
• Parents/legal guardians have provided consent for enrollment

You may not qualify if…

• a major malformation or a neuromuscular condition that affects respiration or causes apnea, or terminal illness or decision to withhold or limit support.

Where it is running

• University of Alabama at Birmingham — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.