Cerebral Hypoxia Clinical Trials

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Optimizing Caffeine Therapy for Hypoxia in Preterm Neonates: A Randomized Trial Assessing Efficacy, Acute Kidney and Brain Injury, Safety, and Pharmacokinetics

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study is being done to see if additional caffeine citrate (20 milligrams per kilogram IV bolus) helps babies with low kidney oxygenation already being treated with caffeine citrate (20 milligrams per kilogram IV bolus on day of life (DOL) 1 followed by 8 milligrams per kilogram daily maintenance). The investigators hypothesize that additional caffeine will improve kidney oxygen levels, while not causing any brain injury, and may reduce rates of acute kidney injury compared to placebo. This study will take place in preterm babies born less than 30 weeks gestational age, with the intervention occurring between greater than 48 hours of age until DOL 14 and outcomes tracked until neonatal intensive care unit (NICU) discharge.

Eligibility
Participation Requirements
Sex: All
Minimum Age: Newborn
Maximum Age: 4 days
Healthy Volunteers: f
View:

• Gestational age at birth between 23 0/7 and 29 6/7 weeks.

• Able to have near-infrared spectroscopy (NIRS) monitoring of cerebral and kidney oxygenation.

• Able to receive IV medications.

• Indwelling umbilical arterial catheter (UAC), umbilical venous catheter (UVC), peripheral arterial line (PAL), or peripherally inserted central catheter (PICC) already in place that can draw blood.

• Receiving caffeine at the time of enrollment

• Have a birth parent who is at least 18 years old and have a parent or guardian who is able to provide parental permission in English or Spanish

Locations
United States
Wisconsin
UW Hospital and Clinics
RECRUITING
Madison
Contact Information
Primary
Elena Alfaro, CCRP
elalfaro@wisc.edu
(608) 890-0584
Time Frame
Start Date: 2026-05-28
Estimated Completion Date: 2030-09
Participants
Target number of participants: 114
Treatments
Experimental: Arm 1: Caffeine
Placebo_comparator: Arm 2: Placebo
No_intervention: Arm 3: Control
Related Therapeutic Areas
Sponsors
Leads: University of Wisconsin, Madison
Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

This content was sourced from clinicaltrials.gov