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.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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