跳至主要内容
临床试验/NCT02028325
NCT02028325终止4 期

Yellow 560 Microscope for Intraoperative Visualization of Fluorescein Stained Intracranial Lesions

Indiana University2 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2013年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
136
试验地点
2
主要终点
Concordance Between Surgical Impression of Residual Lesion and Appearance on Post-operative Imaging

研究概览

简要总结

The purpose of this study is to evaluate the effectiveness of using Fluorescein Sodium and the Yellow 560 microscope to aid in treatment of intracranial tumors and vascular lesions.

详细描述

The purpose of this study is to evaluate the effectiveness of using Fluorescein Sodium and the Yellow 560 microscope to aid in treatment of intracranial tumors and vascular lesions. The objectives of this study aim to investigate the use of Fluorescein in assisting with evaluating complete tumor removal and thorough treatment of intracranial vascular lesions as well as tumor biopsy procedures. The hypothesis is that Fluorescein Sodium will help surgeons better identify residual tumor and vascular lesions and its use will allow surgeons to obtain better surgical results and prognostic outcomes.

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
All
接受健康志愿者

入选标准

  • Age 18 years or older.
  • Diagnosed by preoperative imaging modalities to have a brain tumor or vascular lesions (aneurysm, arteriovenous malformation or arteriovenous fistula) requiring surgical intervention.
  • The patient is determined by a board certified Neurosurgeon (above mentioned neurosurgeons) to benefit from the application of Fluorescein Sodium intraoperatively
  • Patient or legally authorized representative provides written informed consent to enroll in this study.

排除标准

  • Known allergic reaction to Fluorescein Sodium.
  • Children.
  • Prisoners.
  • Students.
  • Infection of the central nervous system or other sites.
  • Hemodynamic instability or significant impairments in circulation.
  • Concomitant treatment with other investigational drugs.
  • Any uncontrolled condition unrelated to the neurosurgical disease.
  • History of psychiatric, additive, or any other disorder that compromises the ability to provide informed consent or comply with study protocols.
  • Participation on other clinical trials during the last thirty days.
  • Pregnant patients.
  • Patients unable to discontinue medications that affect Fluorescein metabolism.

研究组 & 干预措施

Fluorescein Sodium

Experimental

All patients enrolled in the study will prepare for surgery as per standard neurosurgical indications, procedures and institution protocols. At the time of the anesthesia induction, with the patient under general anesthesia, Fluorescein Sodium 10% (100mg/1mL) at a dose of 3-20 mg/kg will be administered intravenously (the optimal dosage will be determined within the study as the most minimal dose for adequate visualization will be used). For vascular lesions, fluorescein sodium 10% (100mg/1mL) will be injected and used to assess its application after the conventional methods have confirmed the exclusion of the aneurysm. No patient's care will be affected by the results of the Fluorescein angiography.

干预措施: Fluorescein Sodium (Drug)

结局指标

主要结局

Concordance Between Surgical Impression of Residual Lesion and Appearance on Post-operative Imaging

时间窗: up to 1 week. For subjects where clinical post-operative MRI/angiography was not performed within 7 days, MRI/angiography completed within 3 months post-operatively was utilized for evaluation.

We will perform fluorescein fluorescence/angiography at surgery and assess if fluorescence reveals any residual tumor or vascular lesion (aneurysm, arteriovenous malformation, or arteriovenous fistula) following surgical intervention. For subjects with brain tumors we will then perform a regular postoperative MRI and assess if there was any residual tumor and measure the accuracy of fluorescein fluorescence to assess the amount of the residual tumor seen on the postoperative MRI. Similarly, for the aneurysms or other vascular lesions, we will perform a regular postoperative angiogram and assess the accuracy of fluorescein angiography results in estimating the amount of residual lesion.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Aaron Cohen-Gadol

Neurosurgeon

Indiana University

研究点 (2)

Loading locations...

相似试验