临床试验/NCT06607731

NCT06607731招募中不适用

Percutaneous Gelled Alcohol Sclerotherapy for Aggressive Angiomas: Evaluation of Feasibility, Safety, and Efficacy

Centre Hospitalier Universitaire de Saint Etienne1 个研究点分布在 1 个国家目标入组 11 人开始时间: 2024年6月25日最近更新: 2024年10月8日

适应症

试验速览

阶段: 不适用
状态: 招募中
发起方: Centre Hospitalier Universitaire de Saint Etienne
入组人数: 11
试验地点: 1
主要终点: Number of complications identified in data collection

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The investigators aimed to evaluate efficacy and safety of a non-surgical protocol treatment combining transarterial embolization and percutaneous radiopaque gelled ethanol (RGE) sclerotherapy in a first procedure, then followed by vertebroplasty in a second procedure, to treat aggressive vertebral hemangioma patients in tertiary hospital. Exclusion criteria were age <18-years old and any association with neurological deficit.

研究设计

研究类型: Observational
观察模型: Cohort
时间视角: Retrospective

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Every patients treated by gelled alcohol sclerotherapy for aggressive angiomas, in the University Hospital of Saint-Etienne.

排除标准

•Patients no treated by gelled alcohol sclerotherapy.

结局指标

主要结局

Number of complications identified in data collection

时间窗: Day 1

Number of complications identified in data collection

次要结局

Number of lesion identified in data collection(Day 1)

研究者

发起方

Centre Hospitalier Universitaire de Saint Etienne

申办方类型

Other

责任方

Sponsor

研究点 (1)

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