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临床试验/NCT01913340
NCT01913340已完成1 期

Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study

University of California, San Francisco7 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
50
试验地点
7
主要终点
Markers of Organ Function

研究概览

简要总结

Hypoxic-ischemic encephalopathy (HIE), a condition of reduced blood and oxygen flow to a baby's brain near the time of birth, may cause death or neurologic disability. Cooling therapy (hypothermia) provides some protection, but about half of affected infants still have a poor outcome. This clinical trial will determine if the drug erythropoietin, given with hypothermia, is safe to use as a treatment that may further reduce the risk of neurologic deficits after HIE.

详细描述

This phase I/II clinical trial is designed to demonstrate:

  1. The feasibility of recruiting, enrolling and following 50 patients with moderate to severe HIE at 5 sites, while meeting specified recruitment and follow-up target goals.
  2. The safety of high-dose Epo therapy in neonates with HIE with respect to systemic organ function and general growth parameters.
  3. The value of brain MRI/MRS performed at 4-7 days of age as a biomarker of motor function at 12 months of age.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
30 Minutes 至 24 Hours(Child)
性别
All
接受健康志愿者

入选标准

  • Newborns ≥ 36 weeks gestation, < 23 hours of age at time of consent, must meet all 3 Inclusion Criteria to be eligible for the study:
  • Perinatal depression = at least one of the following: a) Apgar ≤5 at 10 min or b) required resuscitation (endotracheal or mask ventilation, or chest compressions) at 10 min or c) pH < 7.0 or base deficit ≥15 in cord, arterial, or venous blood obtained at <60 min of age;
  • Moderate to severe encephalopathy = at least 3 of 6 modified Sarnat criteria present between 1-6 h of birth: a) reduced level of consciousness; b) decreased spontaneous activity; c) hypotonia; d) decreased suck; e) decreased Moro reflex; or f) respiratory distress including periodic breathing or apnea; and
  • Hypothermia = passive or active cooling begun by 6 hours of age.

排除标准

  • Intrauterine growth restriction (BW <1800 g);
  • Major congenital malformation; suspected genetic syndrome, metabolic disorder or TORCH infection;
  • Head circumference < 2 SD for gestation;
  • Infant for whom withdrawal of supportive care is being considered; or
  • Anticipated inability to collect primary endpoint at 12 months of age.

研究组 & 干预措施

Erythropoietin

Active Comparator

1000 U/kg/dose x 5 doses

干预措施: Erythropoietin (Drug)

Normal saline

Placebo Comparator

干预措施: Normal saline (Drug)

结局指标

主要结局

Markers of Organ Function

时间窗: Participants will be followed for the duration of hospital stay, an expected average of 2 weeks

The investigators will monitor organ function and adverse events until hospital discharge from the neonatal intensive care unit

次要结局

  • Alberta Infant Motor Scale (AIMS)(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (7)

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