跳至主要内容
临床试验/NCT05672849
NCT05672849招募中不适用

Safety and Efficacy of Devices Used in Fetoscopic Neural Tube Defect Repair Cases

Michael A Belfort2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年11月14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
100
试验地点
2
主要终点
Number of adverse events

研究概览

简要总结

The purpose of the study is to evaluate the safety and efficacy of devices used in patients undergoing fetoscopic neural tube defect repair.

详细描述

All patients who choose to undergo fetoscopic neural tube defect repair at Texas Children's Fetal Center will be offered participation in this research study by study investigators. Description of study rationale and design and a focused interview by the study coordinator to afford potential participants a formal opportunity to examine what they have learned about the research study in the course of their evaluation and discuss how they feel about enrolling in the research study. Once the patient is deemed eligible the informed consent process will be reviewed. If patients elect to participate in the study, informed consent will be obtained, and patients provided a copy of the signed consent.

Fetoscopic Procedure: The fetoscopic open neural tube defect repair procedure will be performed with the same technique in this protocol as the investigators did in the previous protocols under this IDE (NCT02230072 and NCT03794011) in terms of exteriorization of the uterus, preparation for the fetoscopic repair and repair of the open neural tube defect. This involves release of the placode, dissection of the surrounding skin, development of myofascial flaps on either side of the defect, placement of a patch to be laid on top of the placode prior to closure of the myofascial flaps, suture of the flaps over the freed placode and patch and attempted primary closure of the defect using available skin. If necessary, the surgeons will use relaxing incisions or a skin patch to provide additional mobility to the skin to be closed over the defect. If the surgeons are unable to close the skin primarily despite best fetoscopic efforts, the option of performing/completing the repair as an open procedure exists and will be offered to the subject.

Follow-Up: The investigators will follow patients for the immediate post-procedure period (until they leave the OR).

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
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients who elect to undergo fetoscopic neural tube defect repair

排除标准

  • Patients who do not elect to undergo fetoscopic neural tube defect repair

结局指标

主要结局

Number of adverse events

时间窗: Immediate Post-Procedure period (until the leave the OR)

Number of adverse events associated with the investigational device

Number of device defects, malfunctions, or failures

时间窗: Immediate Post-Procedure period (until the leave the OR)

Number of device defects, malfunctions, or failures and whether the device performed as intended.

次要结局

未报告次要终点

研究者

发起方
Michael A Belfort
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Michael A Belfort

Chairman and Professor

Baylor College of Medicine

研究点 (2)

Loading locations...

相似试验

Safety and Efficacy of Devices Used in Fetoscopic... | 临床试验