The purpose of this trial was to find the best dose of N-acetylcysteine (NAC) to decrease brain injury in babies exposed to intrauterine infection without causing significant side effects.
Age range
13 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
NAC Terminal Elimination Half-life
Timeframe: prior to delivery in mothers, and in newborn after delivery during 2 days of NAC infusion
NAC Volume of Distribution
Timeframe: prior to delivery in mothers, and in newborn after delivery during 2 days of NAC infusion
NAC Total Body Clearance
Timeframe: prior to delivery in mothers, and in newborn after delivery during 2 days of NAC infusion
NAC Concentrations
Timeframe: Peak: 30 minutes after NAC infusion. Cord: at delivery
Placental Transfer Ratio
Timeframe: At time of delivery
Maternal and Infant Mean Blood Pressure Change
Timeframe: Maternal mean BP changes were pre/post dosing prior to delivery. Infant measurements were pre/post their first dosing
Cerebral Blood Flow
Timeframe: after NAC infusion
Prothrombin Time
Timeframe: after N-acetylcystiene or saline infusion