Fluorescence Guided Focal Cortical Dysplasia Surgery (FLUOFOCODYS)
Epilepsy is one of the most common neurological disorders, with one of the highest morbidity rates of all diseases. Despite the development of new anticonvulsant drugs, around a third of patients suffer from drug-resistant epilepsy (RPE). The onset of RPE can be lengthy, prolonging the period during which affected patients live with seizures that have a negative impact on their quality of life. Epilepsy surgery can be a curative treatment, and can enable anticonvulsant medication to be discontinued, optimizing quality of life and cognitive development. In addition, as it has been shown that the prolonged duration of epilepsy prior to surgery has an impact on the occurrence of postoperative seizures, early surgery is increasingly being considered. Focal cortical dysplasia (FCD) is the leading cause of focal lesional epilepsy and is generally drug-resistant. Good postoperative seizure results after surgical resection are strongly linked to complete resection of the dysplastic tissue. Consequently, accurate localization and precise delineation of FCD lesions are crucial during surgery. Currently, the extent of surgical resection is based primarily on preoperative examination, as the macroscopic appearance of dysplastic tissue does not differ from normal cortex. The various intraoperative techniques available to improve the quality of excision (neuronavigation, ultrasound, intraoperative MRI and intraoperative guidance by fluorescence microscopy) all have their limitations. In this context, new intraoperative tools are needed to help the neurosurgeon delineate lesions during surgery. Intraoperative fluorescence spectroscopy is used for surgical guidance of gliomas and other brain pathologies, and has demonstrated its ability to characterize pathological tissues. DCFs exhibit metabolic differences that can also be detected by 5-amino-levulinic acid (5-ALA)-induced protoporphyrin IX (PpIX) fluorescence intraoperatively. Indeed, in some patients who underwent surgery after a diagnosis of glioma, fluorescence was observed even though histological analysis classified the excised tissue as DCF. What's more, glioma and DCF share a common feature: the mitochondria of affected cells are deficient in complex IV. Cytochrome c oxidase (CCO) is largely involved in mitochondrial complex IV, and NAD is a central metabolite involved in redox reactions within cells. Both metabolites (CCO and NAD) can be visualized intraoperatively by optical and fluorescence spectroscopy.
FLUOFOCODYS is a prospective, non-comparative, single-center, human drug pilot clinical trial. 5 patients will be included.
研究概览
详细说明
Primary objective of FLUOFOCODYS study is to measure the fluorescence of biomarkers of focal epileptic lesions by intraoperative fluorescence spectroscopy.
The secondary objectives are as follows:
- To compare the measurement of FCD volume between multimodal high-resolution MRI (HRM) and standard MRI.
- To assess the concordance of FCD measurements between multimodal high-resolution MRI (HRM) and standard MRI.
- Evaluate the correlation between fluorescence spectroscopy and SpiderMass measurements on the collected tissue sample.
- Describe any adverse events that occurred after treatment up to the end of study participation.
The hypothesis of this project is that intraoperative fluorescence spectroscopy could robustly measure 5-ALA-induced protoporphyrin IX fluorescence in FCD and could ultimately aid FCD surgery. Thus, to understand intraoperative biomarker fluorescence spectroscopy in DCF, preoperative MRI and postoperative histology are crucial. This will enable MRI-informed intraoperative fluorescence spectroscopy. These comparative measurements will be completed with SpiderMass technology (metabo-lipidomic mass spectrometry). The effectiveness of intraoperative tools could therefore be assessed prior to surgery, which could have an impact on the therapeutic decision to proceed with surgery.
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Pierre-Aurélien BEURIAT, MD
- 电话号码:+33 4 27 85 62 20
- 邮箱:pierre-aurelien.beuriat@chu-lyon.fr
研究联系人备份
- 姓名:Clarisse SAUNIER
- 电话号码:+33 4 27 85 62 64
- 邮箱:clarisse.saunier@chu-lyon.fr
学习地点
-
-
-
Bron、法国、69500
- Hôpital Neurologique Pierre Wertheimer - Groupement Hospitalier Est - Hospices Civils de Lyon
-
接触:
- Marc GUENOT
- 电话号码:+33 4 72 35 71 97
- 邮箱:marc.guenot@chu-lyon.fr
-
首席研究员:
- Marc GUENOT
-
Bron、法国
- Hôpital Femme Mère Enfant - Groupement Hospitalier Est - Hospices Civils de Lyon
-
接触:
- Pierre-Aurélien BEURIAT, MD
- 电话号码:+33 4 27 85 62 20
- 邮箱:pierre.aurelien@chu-lyon.fr
-
首席研究员:
- Pierre-Aurélien BEURIAT, MD
-
-
参与标准
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Patient with drug resistant epilepsy, related to a type II FCD visible on MRI
- Patient with surgical indication validated by the epileptic multi-disciplinary staff meeting
- First FCD surgery
- Signed written informed consent before any study specific intervention
- Patient affiliated to the national health system or benefiting from it
Exclusion Criteria:
- Patients weighing over 75kg
- Patients requiring general anaesthesia for MRI at investigator discretion
- Contra indication to MRI : obesity, claustrophobia, metallic object
- Hypersensitivity to the active substance or to porphyrins
- Acute or chronic porphyria
- For woman of childbearing potential: Pregnancy or breastfeeding or patients who is not willing to comply with the contraceptive requirements during the study period
- Inability to follow the procedures of the study
- Simultaneous enrolment to another study which could influence the results of the current study
- Patient under legal protection or deprived of liberty
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:5-ALA (Gliolan)
Children and adults with drug resistant epilepsy, related to a probable FCD and with surgical indication validated by the epileptic multi-disciplinary staff meeting will receive the study treatment (5-ALA) orally at a dose of 20mg/kg
|
Patients will be given 5-ALA (20 mg per kilogram body weight) before the surgery, between 2 and 4 hours before anaesthesia.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Concentration of fluorescent compound (in mol/L) during the chirurgical intervention on the extracted tissue sample of FCD
大体时间:Day 0
|
Measure of biomarkers fluorescence of focal epileptic lesion by intraoperative fluorescence spectroscopy.
|
Day 0
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
FCD volume in mm3 on standard MRI
大体时间:60 days before Day 0 (=surgery)
|
Compare FCD volume between High Resolution-MultiModal-MRI and standard MRI.
|
60 days before Day 0 (=surgery)
|
|
FCD volume in mm3 on High Resolution MM- MRI
大体时间:Day 0 (=surgery)
|
Compare FCD volume between High Resolution-MultiModal-MRI and standard MRI.
|
Day 0 (=surgery)
|
|
Index kappa concordance of the volume in mm3 of focal cortical dysplasia measured by standard MRI
大体时间:60 days before day 0
|
Evaluation of the concordance of FCD measurements between HR-MM-MRI and standard MRI
|
60 days before day 0
|
|
Index kappa concordance of the volume in mm3 of focal cortical dysplasia measured by HR MM-MRI
大体时间:Day 0
|
Evaluation of the concordance of FCD measurements between HR-MM-MRI and standard MRI
|
Day 0
|
|
Concentration measured by fluorescence spectroscopy on extracted tissue sample of FCD
大体时间:Day 0
|
Evaluation of correlation between fluorescence spectroscopy measurements and Spidermass measurements on extracted tissue sample of FCD.
|
Day 0
|
|
Relative concentration of molecular species measured by SpiderMass on extracted tissue sample of FCD
大体时间:Day 0
|
Evaluation of correlation between fluorescence spectroscopy measurements and Spidermass measurements on extracted tissue sample of FCD.
|
Day 0
|
|
Number of adverse events
大体时间:From the enrollment to day 1
|
Description of any Adverse Events that have occurred after the experimental treatment until end of study participation
|
From the enrollment to day 1
|
合作者和调查者
调查人员
- 首席研究员:Pierre-Aurélien BEURIAT、Hospices Civils de Lyon
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 69HCL24_0906
- 2025-523608-64-00 (克蒂斯)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.