Theophylline Prophylaxis During Hypothermia to Limit Neonatal Nephron Damage
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Recruitment of patients
研究概览
简要总结
Acute kidney injury is a significant complication for infants who experience hypoxic ischemic encephalopathy, being associated with increased rates of death and prolonged hospitalization. This pilot study of theophylline administration soon after birth for the prevention of kidney injury will lay the foundation for the conduct of a larger clinical trial that seeks to identify a theophylline as a novel therapy to prevent kidney injury in thousands of at-risk infants.
详细描述
Acute kidney injury (AKI) is commonly seen in infants diagnosed with hypoxic-ischemic encephalopathy (HIE) and is associated with increased rates of morbidity and mortality. Currently, there are no approved therapies that target the prevention of AKI. Several small trials in infants with HIE suggest that a single dose of theophylline given soon after birth attenuates the development of AKI. However, these studies were not performed in infants being treated with therapeutic hypothermia (the current standard of care for moderate to severe HIE), and only reported short-term outcomes. Therefore, few clinicians use theophylline in the management of these patients. The long-term goal is to undertake an appropriately powered multicenter clinical trial to test the hypothesis that for infants > 35 weeks gestation treated with therapeutic hypothermia for HIE, intravenous theophylline (or aminophylline) within the first 18 hours after birth will result in a decreased incidence and/or severity of AKI or death (composite primary outcome) and improved long-term (2 year) renal outcomes. Before the conduct of a large trial, the feasibility of implementing the intervention and ability to measure relevant clinical outcomes need to be demonstrated. Therefore, the investigators propose a small pilot and feasibility clinical trial to i) evaluate recruitment, protocol adherence, and data collection procedures in a therapeutic trial of theophylline to decrease the incidence of AKI or death compared to standard treatment in infants with HIE being treated with therapeutic hypothermia; ii) evaluate the utility and applicability of established measures (serum creatinine, urine output, fluid balance) and novel, exploratory approaches to identify AKI in infants; and iii) determine theophylline pharmacokinetic, pharmacodynamic, safety and preliminary effectiveness profiles of two different theophylline dosing regimens in a therapeutic trial of theophylline to decrease the incidence of AKI or death compared to standard treatment. Using a mixed methods data analysis strategy to assess the research and intervention process and examine outcomes of the intervention, the investigators will generate the requisite data to inform development and implementation of an appropriately powered study to determine whether theophylline attenuates the risk and severity of AKI in infants with HIE treated with therapeutic hypothermia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 1 Hour 至 18 Hours(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •gestational age at birth >= 35 weeks by best obstetrical dating
- •birth weight > 1800 grams
- •clinical determination of HIE and treatment with hypothermia being initiated within six hours of birth according to institutional guidelines
- •no known congenital abnormalities involving the brain, kidneys, heart or lungs
- •ability to administer theophylline via intravenous route within 18 hours of birth
排除标准
- •infants with suspected or diagnosed significant renal, urinary tract, brain, heart, or lung abnormalities
- •infant with known chromosomal anomaly
- •evidence of head trauma or skull fracture causing major intracranial hemorrhage
- •inability to initiate hypothermia within six hours of birth
- •attending physician unwilling to have infant participate in the study
- •inability to obtain informed consent within 18 hours of birth
研究组 & 干预措施
Standard treatment
Infants cared for according to standard practice.
Single Dose Theophylline
Single dose of theophylline or aminophylline (5mg/kg IV) given within 18 hours after birth
干预措施: Single Dose Theophylline (Drug)
Repeat Dose Theophylline
Loading dose of theophylline or aminophylline (5mg/kg IV) given within 18 hours of birth, with two subsequent doses (1.2 mg/kg IV) given at 12 and 24 hours after the loading dose
干预措施: Repeat Dose Theophylline (Drug)
结局指标
主要结局
Recruitment of patients
时间窗: 2 years
Examine the ability to recruit and enroll patients in trial. We will assess the number of eligible patients and compare that number to those actually enrolled. This ratio will inform regarding the ability to recruit patients in a larger, randomized, appropriately powered trial.
次要结局
- Pharmacokinetic Profile of Theophylline#1(2 years)
- Safety profile of theophylline#1(2 years)
- Safety profile of theophylline#2(2 years)
- Safety profile of theophylline#3(2 years)
- Demonstration of successful adherence to study protocol(2 years)
- Successful data collection procedures(2 years)
- Successful biospecimen collection procedures(2 years)
- Pharmacokinetic Profile of Theophylline#2(2 years)
- Acute kidney injury#1(2 years)
- Acute kidney injury#2(2 years)
研究者
Jeffrey Segar
Professor, Department of Pediatrics
Medical College of Wisconsin
