跳至主要内容
临床试验/NCT00451698
NCT00451698终止不适用

Erythropoietin and Pediatric Cardiac Surgery

Medical College of Wisconsin1 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2007年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
9
试验地点
1
主要终点
Biochemical Markers of Heart Damage

研究概览

简要总结

Lack of bloodflow to the heart and brain when the heart is stopped during heart surgery can cause damage to those organs. We hypothesize that a single dose of erythropoietin prior to the heart bypass portion of surgery may protect the infant human heart and brain from injury.

This randomized clinical trial will involve 120 children, age 6 weeks to 18 years, requiring heart bypass surgery for congenital heart defects.

详细描述

Lack of bloodflow to the heart and brain when the heart is stopped during heart surgery can cause damage to those organs. A medicine already used in humans, erythropoietin, may protect the heart and brain of children born with heart defects during their surgical repair. In a rabbit model, erythropoietin did protect the hearts. We hypothesize that a single dose of erythropoietin prior to the heart bypass portion of surgery may protect the infant human heart and brain from injury.

For this randomized control trial, 120 children, age 6 weeks to 18 years, requiring heart bypass surgery for congenital heart defects, will be divided into four groups. Two groups will be children whose usual blood oxygen level is low because of their heart defect; the other two will be children with normal blood oxygen levels. Each child will be randomized to receive either erythropoietin or placebo 15 minutes prior to stopping the heart during their surgery.

Erythropoietin's protective function will be measured after surgery by: (1) amount of medication required to support heart function, (2) how well the heart pumps blood as seen by echocardiogram, (3) levels of chemicals produced by the body when heart or brain tissue injury occurs, (4) urine output and oxygen levels (5) time on ventilator support (6) ICU stay and (7) hospital stay. Heart tissue will be collected during surgery to determine how erythropoietin protects heart cells.

Statistical tests including ANOVA will test for similarities and differences among the groups on the measures of protection from injury.

Note - the study design was edited after the FDA released a warning about the use of erythropoietin. Only acyanotic patients were recruited therefore only 2 study groups are included.

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
6 Weeks 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Age 6 weeks to 18 years
  • Requiring open heart surgery for congenital heart defect -Parents able to speak English and document informed consent -

排除标准

  • Received erythropoietin within past 30 days
  • Previous adverse reaction to erythropoietin or to albumin
  • History of neurological disorder -Laboratory evidence of kidney or liver dysfunction -

研究组 & 干预措施

3

Placebo Comparator

acyanotic placebo

干预措施: acyanotic placebo (Drug)

4

Experimental

acyanotic erythropoietin

干预措施: acyanotic erythropoietin (Drug)

结局指标

主要结局

Biochemical Markers of Heart Damage

时间窗: 4 postoperative time points up to 48 hours

Troponin I levels (ng/ml) measured at 4 time points

Biochemical Markers of Neuron Damage

时间窗: 4 postoperative time points

Echocardiographic Assessment of Heart Function

时间窗: 24 hours postop

次要结局

  • Inotropic Support(24 and 48 hours post operative)
  • Length of Hospitalization(At hospital discharge, up to 30 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验