跳至主要内容
临床试验/NCT06929572
NCT06929572招募中不适用

Autologous Human Umbilical Cord Tissue Patch for Postnatal Closure of Open Neural Tube Defects

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2025年8月5日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
15
试验地点
2
主要终点
Number of participants that have wound dehiscence

研究概览

简要总结

The purpose of this study is to determine the impact of an autologous umbilical cord patch for dural closure on the repair of open neural tube defect. The outcomes will evaluate successful defect closure, creation of a more capacious spinal canal, and reduction in inflammatory tissue response versus historical controls.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Neonates born with prenatal diagnosis of open neural tube defect (myelomeningocele or myeloschisis)
  • Resident of the United States
  • Provision of signed and dated informed consent form
  • Stated willingness by legally authorized representative (LAR) to comply with all study procedures and availability for the duration of the study
  • Maternal age 18 years and older
  • Mother is English or Spanish Speaking

排除标准

  • Sepsis or signs of infection of the neonate
  • Febrile or other acute illness of the neonate at time of delivery
  • Major congenital anomaly unrelated to spina bifida that may impact safety of neonate for surgery
  • Evidence of intra-amniotic or maternal infection related to pregnancy at time of delivery
  • Maternal use of steroid therapy during pregnancy or neonate use of steroid therapy,except for lung maturity indications
  • Vaginal delivery
  • Patch closure of dura is deemed unnecessary
  • Umbilical cord abnormality
  • Insufficient autologous cord tissue or patch
  • Autologous umbilical cord patch that does not meet laboratory safety standards per standard operating procedure (SOP)
  • Treatment with an investigational drug or other intervention that would influence morbidity or mortality

结局指标

主要结局

Number of participants that have wound dehiscence

时间窗: 1-year post-op

Number of participants that have Cerebrospinal fluid (CSF) leakage

时间窗: one-month post-op

Number of participants that have CSF leakage

时间窗: 1-year post-op.

次要结局

  • Number of participants that present with tethered cord syndrome(one-month post-op,12-months post-op, 30-months post-op, and 60-months post-op)
  • Number of participants that had a change in level of neurological function as assessed by the American Spinal Injury Association Impairment Scale (ASIA)(baseline, one-month post-op,12-months post-op)

研究者

发起方
The University of Texas Health Science Center, Houston
申办方类型
Other
责任方
Principal Investigator
主要研究者

Stephen Fletcher

Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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