Recruiting
Phase 2

Caffeine Citrate

Sponsor:

University of Rochester

Code:

NCT07216365

Conditions

Neonatal Apnea

Infants

Eligibility Criteria

Sex: All

Age: 0

Healthy Volunteers: Not accepted

Interventions

Caffeine Citrate

Study Details

Brief summary:

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.

Conditions

Neonatal Apnea

Infants

Study ID

NCT07216365

Start date

Jul 15, 2026

Status verified date

Jul, 2026

Completion date

Sep 1, 2029

Anticipated

Primary completion date

Jul 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • URMC Inborn Newborn infants born with gestational age of 22 weeks 0 days - 27 weeks 6 days or infants OR ≥ 28 weeks with a birthweight < 1000 grams

Exclusion Criteria:

  • Hepatic failure, spontaneous intestinal perforation, necrotizing enterocolitis, Anticipated major congenital or genetic anomalies, infants not anticipated to survive beyond 72 hours, infants with mothers that are non-English speaking or <18 years old at time of enrollment.

Study Design

Enrollment

40 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: High Dose Caffeine Arm

Infants randomized to the high dose caffeine arm will receive an initial standard loading dose of 20 mg/kg caffeine citrate. Beginning at 7 days of life, they will receive a maintenance dose of 10 mg/kg/day caffeine citrate. Dose escalation may be performed at the discretion of the clinical team, with a maximum maintenance dose of 12.5 mg/kg/day if clinically indicated. Caffeine will be administered IV or PO at a 1:1 ratio and prepared in a blinded fashion.

active comparator: Standard Dose Caffeine Arm

Infants randomized to the standard dose caffeine arm will receive an initial loading dose of 20 mg/kg caffeine citrate. Beginning at 7 days of life, they will receive a maintenance dose of 5 mg/kg/day. Dose escalation may occur at the discretion of the clinical team, with a maximum maintenance dose of 7.5 mg/kg/day. Caffeine will be administered IV or PO at a 1:1 ratio and prepared in a blinded fashion.

Interventions

Caffeine Citrate

High Dose Group:

Caffeine citrate administered as a 20 mg/kg loading dose followed by a 10 mg/kg/day maintenance dose starting at 7 days of life. Dose escalation up to 12.5 mg/kg/day may be performed based on clinical indications. The drug is administered either intravenously or orally in a blinded fashion.

Standard Dose Group:

Caffeine citrate administered as a 20 mg/kg loading dose followed by a 5 mg/kg/day maintenance dose starting at 7 days of life. Dose escalation up to 7.5 mg/kg/day may be performed based on clinical indications. The drug is administered either intravenously or orally in a blinded fashion.

Primary outcome measure

  • Average Oxygen Saturation Index (OSI) per Patient Over First 56 Days [ Time Frame: From Randomization to Day 56 or Caffeine Discontinuation ]
  • Total Duration of Respiratory Support [ Time Frame: From Randomization to 1 year ]
  • Total Incidence of Severe Bronchopulmonary Dysplasia (BPD) [ Time Frame: From Randomization to 1 year ]
  • Total Incidence of Severe Intraventricular Hemorrhage or Periventricular Leukomalacia (IVH/PVL) [ Time Frame: From Randomization to 1 year ]
  • Total Length of NICU Stay [ Time Frame: Birth to 1 year ]
  • Total Number of Infant Deaths [ Time Frame: From Randomization to 1 year ]
  • Total Test of Infant Motor Performance (TIMP) Score Prior to Discharge [ Time Frame: Prior to NICU Discharge ]
  • Total Duration of SpO₂ Below Threshold (Intermittent Hypoxia) [ Time Frame: From Randomization through Day 56 ]
  • Total Time with Heart Rate >180 bpm (Tachycardia) [ Time Frame: From Randomization to 1 year ]
  • Total Growth Parameter Z-Scores (Length, Weight, Head Circumference) [ Time Frame: From Randomization to 1 year ]
  • Total Osteopenia Markers (Alkaline Phosphatase, Calcium, Phosphorus) [ Time Frame: From Randomization to 1 year ]
  • Total Incidence of Hypertension (>95th Percentile) [ Time Frame: From Randomization to 1 year ]
  • Total Time to Full Enteral Feeds [ Time Frame: From Randomization to 1 year ]
  • Total Number of NPO Periods >24 Hours [ Time Frame: From Randomization through NICU Discharge ]
  • Total Incidence of Necrotizing Enterocolitis (NEC) [ Time Frame: From Randomization to 1 year ]
  • Total Incidence of Spontaneous Intestinal Perforation (SIP) [ Time Frame: From Randomization to 1 year ]

Central Contacts and Locations

Central contacts

Locations

University of Rochester Medical Center

Recruiting

Rochester, New York, United States, 14642

Contacts

More Information

Sponsor

University of Rochester

Last update posted

Jul 29, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Rochester on 2026-07-29.