Complex Oro-Facial Pain: Functional Imaging Characterization and Treatment With Transcranial Magnetic Stimulation
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 9
- 试验地点
- 2
- 主要终点
- Visual Analogue Scale (VAS)
研究概览
简要总结
Complex oro-facial pain is a poorly diagnosed and poorly treated cause of significant suffering and disability. This study will explore the ability of fMRI to identify patients with complex oro-facial pain who respond to transcranial magnetic stimulation therapy.
Specific Aims:
- To establish baseline patterns of MRI in patients with chronic oro-facial pain without a definitive etiologic diagnosis.
- To estimate the rate of treatment success of transcranial stimulation of the primary motor cortex (M1) in these patients.
- To identify post-treatment MRI patterns that are associated with treatment success.
详细描述
Methods: Patients diagnosed with complex oral or facial pain at the UMPhysicians Complex Facial Pain Clinic who meet inclusion and exclusion criteria will be offered participation in the study. They will undergo baseline evaluation for depression with the HAM-D and MADRAS scales and for quality of life with the WHOQOL-BREF scale. Pain will be assessed using a 10 point visual analogue scale. Resting and pcasl MRI will be done within 24 hours before the first treatment. Treatment will consist of five daily sessions of motor cortex stimulation contralateral to the pain. Visual analogue pain scores will be obtained just before each treatment. Rating scales, resting and pcasl MRI will be repeated within 24 hours and at 2 weeks after the last treatment. Analysis: FMRI activation patterns will be examined by the investigators and correlated with treatment outcomes with the goal of identifying fMRI characteristics that can select patients suitable for further study.
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 110 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age between 18 and 110
- •Diagnosis of complex oro-facial pain made by the UMPhysicians Complex Facial Pain Clinic
- •Alternative treatment of proven value not available as judged by the UMPhysicians Complex Facial Pain clinic
- •One of the following types of facial pain as assessed by the Burchiel Patient Pain Rating Classification Questionnaire:
- •trigeminal neuralgia Type 2 (TN2)
- •trigeminal neuropathic pain (TNP)
- •trigeminal deafferentation pain (TDP)
- •post herpetic neuralgia (PHN)
- •atypical facial pain (AFP)
- •nervus intermedius neuralgia (NIN)
- •Willing and able to give informed consent
排除标准
- •Subject diagnosed according to the MINI as suffering from any other major Axis I disorder, such as Psychotic Disorder, Bipolar affective disorder, OCD (MDD is not contraindicated when Hamilton Depression Rating Scale -21≤26, or Beck Depression Inventory).
- •Subjects with significant suicidal risk as assessed by the investigator using the Beck Suicide Ideation scale, psychiatric interview or a history of attempted suicide in the past year.
- •Subject has a history of epilepsy or seizure (EXCEPT those therapeutically induced by ECT).
- •Subject has a history of significant head trauma with loss of consciousness for longer than 5 minutes.
- •Subject has a history of cranial surgery within 1 month of treatment.
- •Subject has metallic particles in the eye or head (exclusive of mouth), implanted cardiac pacemaker or any intra-cardiac lines, implanted neurostimulators, intra-cranial implants (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or electrodes) or implanted medical pumps.
- •Subject cannot pass the TMS Adult Safety Screen or the CMRR Safety Screen.
- •Subject has severe and frequent headaches not part of their facial pain syndrome.
- •Subject has a history of significant hearing loss.
- •Subjects with a significant neurological disorder or insult including, but not limited to:
- •Any condition likely to be associated with increased intracranial pressure
- •Space occupying brain lesion
- •History of cerebrovascular accident
- •Transient ischemic attack within two years
- •Cerebral aneurysm
- •MMSE ≤ 24
- •Parkinson's disease
- •Huntington's chorea
- •Multiple sclerosis
- •Subject with a history of substance abuse including alcoholism within the past 6 months (except nicotine and caffeine).
- •Inadequate communication with the patient.
- •Subject is under custodial care.
- •Subject is currently participating in another clinical study or enrolled in another clinical study within 30 days prior to this study.
- •Subject with unstable physical disease such as unstable cardiac disease.
- •Subject is currently on Benzodiazepine at a dose higher than 3 mg of Lorazepam or equivalent.
- •Subject has had previous treatment with TMS.
- •Women who are breast-feeding.
- •Women of childbearing potential and not using a medically accepted form of contraception when sexually active.
- •Inability to give informed consent
结局指标
主要结局
Visual Analogue Scale (VAS)
时间窗: 7 days
Participants are asked to rate pain on a100 mm visual analogue scale with 0 representing no pain and 100 representing worst possible pain. The mean difference from baseline to 7 days post-treatment is recorded.
次要结局
- World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Psychological Health(baseline, 3 and 7 days post treatment)
- World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Physical Health(baseline, 3 and 7 days post treatment)
- World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Environment(baseline, 3 and 7 days post treatment)
- World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Overall(pre-treatment, 3 and 7 days post treatment)
- World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Social Relationships(baseline, 3 and 7 days post treatment)