The goal of this clinical trial is to determine whether a higher dose of caffeine citrate can improve breathing and reduce health complications in extremely premature infants, specifically those born before 28 weeks of pregnancy, known as ELGAN infants. These babies often struggle with breathing due to underdeveloped lungs, and caffeine is commonly used to help support their respiratory function. However, the most effective and safest dose has not yet been clearly established. The study aims to answer two main questions: Does a higher maintenance dose of caffeine (10 mg/kg) lead to better oxygenation, as measured by the Oxygen Saturation Index (OSI), compared to the standard dose (5 mg/kg)? And does the higher dose reduce the risk of serious complications such as lung disease, brain injury, or death-without causing more side effects like fast heart rate, high blood pressure, or poor growth? To answer these questions, researchers will compare two groups of infants: one receiving the high-dose caffeine treatment and the other receiving the standard dose. This comparison will help determine if the higher dose leads to better outcomes without increased risk. Participants will begin caffeine treatment once they have regained their birth weight and are at least seven days old. They will be randomly assigned to receive either the high or standard caffeine dose and will be followed until caffeine is stopped or they are discharged from the hospital. During this time, researchers will monitor each infant's oxygenation levels, need for breathing support, signs of common complications, growth and feeding progress, and any side effects. Before discharge, each infant's motor development will also be assessed using a tool called the Test of Infant Motor Performance (TIMP). This study could help define the most effective caffeine dosing strategy for supporting extremely premature infants and improving their short-term health outcomes.
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Average Oxygen Saturation Index (OSI) per Patient Over First 56 Days
Timeframe: From Randomization to Day 56 or Caffeine Discontinuation
Total Duration of Respiratory Support
Timeframe: From Randomization to 1 year
Total Incidence of Severe Bronchopulmonary Dysplasia (BPD)
Timeframe: From Randomization to 1 year
Total Incidence of Severe Intraventricular Hemorrhage or Periventricular Leukomalacia (IVH/PVL)
Timeframe: From Randomization to 1 year
Total Length of NICU Stay
Timeframe: Birth to 1 year
Total Number of Infant Deaths
Timeframe: From Randomization to 1 year
Total Test of Infant Motor Performance (TIMP) Score Prior to Discharge
Timeframe: Prior to NICU Discharge
Total Duration of SpOâ‚‚ Below Threshold (Intermittent Hypoxia)
Timeframe: From Randomization through Day 56
Total Time with Heart Rate >180 bpm (Tachycardia)
Timeframe: From Randomization to 1 year
Total Growth Parameter Z-Scores (Length, Weight, Head Circumference)
Timeframe: From Randomization to 1 year
Total Osteopenia Markers (Alkaline Phosphatase, Calcium, Phosphorus)
Timeframe: From Randomization to 1 year
Total Incidence of Hypertension (>95th Percentile)
Timeframe: From Randomization to 1 year
Total Time to Full Enteral Feeds
Timeframe: From Randomization to 1 year
Total Number of NPO Periods >24 Hours
Timeframe: From Randomization through NICU Discharge
Total Incidence of Necrotizing Enterocolitis (NEC)
Timeframe: From Randomization to 1 year
Total Incidence of Spontaneous Intestinal Perforation (SIP)
Timeframe: From Randomization to 1 year