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临床试验/CTRI/2025/12/098980
CTRI/2025/12/098980尚未招募不适用

Efficacy of Early Prophylactic Caffeine Vs Therapeutic Caffeine in Neonates 32 weeks Gestation A Randomized Controlled Trial

Dr. Neelam Kler1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年12月22日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
80
试验地点
1

研究概览

简要总结

Caffeine is the standard pharmacologic therapy for apnea of prematurity, with proven benefits in reducing bronchopulmonary dysplasia, facilitating extubation, and improving neurodevelopment. Emerging evidence suggests that early prophylactic caffeine may further reduce respiratory morbidity in preterm neonates . However, most previous studies classified ‘early’ caffeine as administration within 24–72 hours, an interval that overlaps substantially with therapeutic use, potentially diluting the true benefit of early prophylactic administration.

We propose a prospective, open-label, randomized controlled trial in preterm infants <32 weeks gestation to compare early prophylactic caffeine (within 2 h of birth) with therapeutic caffeine (administered peri-extubation or for apnea of prematurity). The primary outcome will be time to discontinuation of respiratory support.. Secondary outcomes will include time to discontinuation of initial invasive ventilation, echocardiographic parameters (left ventricular output, right ventricular output, superior vena cava flow, superior mesenteric artery doppler and anterior cerebral artery doppler at admission, 4 hours of life and 24-36 hours of life), cumulative duration of respiratory support during the hospital stay, bronchopulmonary dysplasia, hemodynamically significant patent ductus arteriosus, necrotizing enterocolitis, severe intraventricular haemorrhage, periventricular leukomalacia, retinopathy of prematurity, growth velocity, neonatal sepsis, use of post-natal steroids, duration of hospital stay and all cause mortality.

We plan to enroll 80 infants (40 per arm). We expect that early prophylactic caffeine will shorten the duration of respiratory support in preterm infants<32 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
0.00 Day(s) 至 1.00 Day(s)(—)
性别
All

入选标准

  • All intramural preterm neonates less than 32 weeks gestation on respiratory support at birth.

排除标准

  • Gestational age less than 24 weeks.
  • Major congenital anomalies or known genetic/syndromic disorders.
  • Antenatally diagnosed congenital diaphragmatic hernia or severe pulmonary hypo- plasia.
  • Requiring chest compressions and/or medications at birth (adrenaline or volume bolus for resuscitation).
  • Failure to obtain consent.

研究者

发起方
Dr. Neelam Kler
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Neelam Kler

Sir Ganga Ram Hospital

研究点 (1)

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