Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05454332

The Caffeine Therapy in the Fetal to Neonatal Transition

Introduction: The caffeine is used in the treatment for apnea of prematurity and it has several positive effects in the neurodevelopment of preterm babies. There are innumerable observational studies suggesting that initiating caffeine in the first hours of life may offer more benefits in the reduction of the necessity of intubation and in ventilation time. It is necessary to expand further research on the best time to start caffeine, which may improve the quality of care for premature infants.

Objective: To evaluate the benefits of caffeine administration in the first two hours of life compared to administration at 24 hours of life in premature patients on noninvasive mechanical ventilation with birth weights less than 1250 grams.

Methodology: Preterm newborn patients with birth weight < 1250 grams born at Hospital de Clínicas de Porto Alegre who are not intubated in the delivery room will be included. Patients will be randomized into two groups. One arm of the study will receive caffeine at 2 hours of age and the other arm will receive caffeine at 24 hours of age (control). Patients in the control group will receive 0.9% SF at 2 hours of life in order to keep the study blinded. The following outcomes will be evaluated: need for intubation, time on invasive and non-invasive mechanical ventilation, BPD, necrotizing enterocolitis, need for ROP treatment, PDA with hemodynamic repercussions, peri-intraventricular hemorrhage, leukomalacia and death. The sample size calculation is 50 patients, 25 in each arm.

Expected Results: It is expected to find a 43% reduction in the need for intubation in preterm infants who receive caffeine in the first two hours of life compared to administration at 24 hours of life. It is also expected to find a reduction in mechanical ventilation time, in addition to a possible reduction in negative outcomes associated with prematurity.

Recruiting

Interested in participating?

Request Info

Key information

Age range

Up to 2 hour

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Hospital de Clínicas de Porto Alegre

Porto Alegre, Rio Grande do Sul, 90035-903, Brazil

Location status: Recruiting

Location contact

Gabriela Trindade

CONTACT

[email protected]

+55 51 985002009

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Premature newborns with birth weight less than 1250 grams
  • Who are not intubated in the delivery room

Exclusion criteria

  • Premature newborns from other hospitals
  • Presence of a major congenital malformation or genetic syndrome

Treatment and study plan

Early Caffeine administration

Drug

Blinding will be done with the administration of saline solution. Patients in the early caffeine group will receive an attack dose of caffeine 20 mg/kg and begin maintenance dose 10 mg/kg/day. Patients in the late caffeine group, receive bolus of saline solution in the first 2 hours of life, starting, at 24 hours of life, the caffeine-loading dose 20 mg/kg and after maintenance dose 10mg/kg/day. The medical team will prescribe the medication, and the pharmacy will be responsible for randomly dispensing the caffeine or saline solution. The pharmacy will prepare syringes with the medication or saline solution identified by a code referring to the randomization without identifying which solution is being administered. The syringes will be sent to the neonatal ICU and will be administered according to the physician's prescription. The administration will be blinded.

Control Group

Other

Blinding will be done with the administration of saline solution. Patients in the early caffeine group will receive an attack dose of caffeine 20 mg/kg and begin maintenance dose 10 mg/kg/day. Patients in the late caffeine group, receive bolus of saline solution in the first 2 hours of life, starting, at 24 hours of life, the caffeine-loading dose 20 mg/kg and after maintenance dose 10mg/kg/day. The medical team will prescribe the medication, and the pharmacy will be responsible for randomly dispensing the caffeine or saline solution. The pharmacy will prepare syringes with the medication or saline solution identified by a code referring to the randomization without identifying which solution is being administered. The syringes will be sent to the neonatal ICU and will be administered according to the physician's prescription. The administration will be blinded.

Primary outcomes

  1. Necessity of intubation

    Time frame: first week of life

    Noninvasive ventilation failure will be defined as intubation in the first seven days of life with the need for invasive ventilation for at least 24 hours.

Secondary outcomes

  1. mechanical ventilation time

    Time frame: until first successful extubation (followed up at least until 36 weeks of corrected age, discharge or death)

    Mechanical ventilation time will be counted until first successful extubation (at least 24 hours extubated)

  2. Number of Participants with Bronchopulmonary dysplasia

    Time frame: followed up at least until 36 weeks of corrected age, discharge or death.

    Bronchopulmonary dysplasia will be defined as need for O2 or ventilatory support at 36 weeks corrected gestational age.

  3. Number of Participants with Intracranial hemorrhage

    Time frame: followed up at least until 36 weeks of corrected age, discharge or death.

    Intracranial hemorrhage will be defined as intracranial hemorrhage grade 3.

  4. Number of Participants with Retinopathy of prematurity

    Time frame: followed up at least until 36 weeks of corrected age, discharge or death.

    Retinopathy of prematurity will be defined with ROP requiring treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

Gabriela Trindade

CONTACT

[email protected]

+55 51 985002009

Sponsors and collaborators

Lead sponsor

Hospital de Clinicas de Porto Alegre

Other

Registry information

Official study title

The Caffeine Therapy in the Fetal to Neonatal Transition in Preterms

Important dates

Study start
2022
Primary completion
2025
Study completion
2026
First posted
Jul 12, 2022
Registry last updated
Apr 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.