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临床试验/NCT03154307
NCT03154307终止不适用

Repeated TMS at Low Frequencies to Reduce Seizure Occurrence

Baptist Health South Florida2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2016年2月19日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
2
试验地点
2
主要终点
Average Weekly Seizure Frequency

研究概览

简要总结

Perform non-invasive neuro-navigated repeated Transcranial Magnetic Stimulation (rTMS) at low frequencies (LF) with the intent to reduce the occurrence of seizures over time (long-term protocol). Seizure reduction and improvements in the quality of life in patients with epilepsy will be associated with increased cortical inhibition resulting from the LF-rTMS sessions over time. This procedure using rTMS at low frequencies (LF-rTMS) between 0.5 and 1 Hz is a safe and painless method for noninvasive focal cortical brain stimulation, which will be evaluated in its efficacy at reducing/suppressing seizures. Accordingly, we propose a clinical trial in patients with epilepsy to test whether LF-rTMS can improve seizure suppression. The location of the presumed 3D source in the brain will be stimulated for few minutes (10 to 15 min.). With the same rTMS modality, we will also perform motor threshold mapping in conjunction with its fully integrated and compatible electroencephalography (EEG) module. Up to 100 individuals 18 to 80 years with epilepsy will be enrolled.

In addition, a short-term protocol has been added to test whether LF-rTMS can reduce or suppress status epilepticus in medically refractory participants.

详细描述

Long term protocol: Perform non-invasive neuro-navigated repeated Transcranial Magnetic Stimulation (rTMS) at low frequencies (LF) with to reduce the occurrence of seizures over time. Seizure reduction and improvements in the quality of life in patients with epilepsy will be associated with increased cortical inhibition resulting from the LF-rTMS sessions over time. This procedure using rTMS at low frequencies (LF-rTMS) between 0.5 and 1 Hz is a safe and painless method for noninvasive focal cortical brain stimulation, which will be evaluated in its efficacy at reducing/suppressing seizures. Accordingly, we propose a clinical trial in patients with epilepsy to test whether LF-rTMS can improve seizure suppression. The location of the presumed 3D source in the brain will be stimulated for few minutes (10 to 15 min.). Using a double-blinded, sham-controlled design, we will enroll up to 100 participants aged 18-80 with focal and generalized retractable epilepsy. Baseline data will include a detailed seizure diary over 4 weeks, psychometric testing/neuropsychology evaluation, and 20-minute EEG recordings. Each patient will then begin treatment with 14 minute sessions of 1 Hz rTMS or sham rTMS, 120%MT, and 800 stimuli on the position of the calculated 3D source using EEG, MRI, and digitized electrode locations. The protocol will be divided in 3 groups (Groups 1, 2 and 3) as follows:

  • Groups 1, 2, and 3: LF-rTMS for 2 weeks (5 days per week for total of 10 days).
  • Group 1: protocol total duration: 1 year: LF-rTMS 1 session/week for 1 month (4 days), and LF-rTMS 1 session/month for 11 months
  • Group 2: protocol total duration: 1 year: LF-rTMS 1 session/month for 12 months
  • Group 3 (placebo protocol, total duration: 1 year): LF-rTMS 1 session/week for 1 month (4 days); and LF-rTMS 1session/month.

During each session EEG may be recorded. Also, we will obtain the number, frequency, and duration of seizure events from an ongoing seizure diary. Psychometric testing will be performed at the beginning of study, 3 months, and at the end of the study. Thus, each patient will have rTMS testing, psychometrics, and EEG recordings. With the same rTMS modality, we will also perform motor threshold mapping in conjunction with its fully integrated and compatible electroencephalography (EEG) module.

Short-term protocol: Use LF-rTMS protocol as described but for up to 5 days in 10 participants with medically refractory status epilepticus. During each session EEG will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Participant and outcomes assessor will be masked in the 3 arms of the long-term protocol. However, the short-term arm will be open label.

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Long-term protocol:
  • Inclusion Criteria:
  • Experience ≥ 3 seizures/month in the month prior to starting study (any type of seizure will count)
  • No status epilepticus in the last 12 months
  • No change in medication in last 30 days

排除标准

  • Presence of implanted electronic devices (e.g., pacemaker, medication pump, brain or vagus nerve stimulator, cochlear implant)
  • Presence of intracranial metal (e.g., aneurysm clip)
  • Unable to cooperate with non-sedated, navigated TMS testing
  • Short-term protocol:
  • Inclusion Criteria:
  • Epilepsia partialis continua or status epilepticus
  • At least 2 medications failed
  • At least 24 hours of acute phase
  • Exclusion Criteria:
  • Presence of implanted electronic devices (e.g., pacemaker, medication pump, brain or vagus nerve stimulator, cochlear implant)
  • Presence of intracranial metal (e.g., aneurysm clip)

结局指标

主要结局

Average Weekly Seizure Frequency

时间窗: 6 and 7 weeks post rTMS treatment

Seizure frequency was recorded by the caregiver in a journal at weeks 6 and 7 post rTMS treatment.

Seizure Duration Proxy for Seizure Severity

时间窗: 6-7-weeks post rTMS treatment

Care provider journaled the seizure duration over the coure of a 2-week period beginning on week 6 post rTMS treatment.

Scalp EEG: Number of Interictal Epileptiform Discharges

时间窗: From start of intervention through 5 days of treatment

Interictal discharges are common in those with epilepsy and tends to decrease with treatment.

次要结局

  • Scalp EEG Functional Connectivity for Alpha Hz(8-weeks Post rTMS Treatment)
  • Treatment Response Rate(8-weeks post rTMS treatment)
  • Abductor Pollicis Brevis (APB)-Evoked Response Threshold(8-weeks Post rTMS treatment)
  • Interhemispheric EEG Asymmetry Ratio for Alpha Power(8-weeks Post rTMS Treatment)
  • Intrahemispheric EEG Asymmetry Ratio for Alpha Power(8-weeks Post rTMS Treatment)

研究者

发起方
Baptist Health South Florida
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alberto Pinzon, M.D.

Neurologist, Medical Director, Baptist Health Epilepsy Program

Baptist Health South Florida

研究点 (2)

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