Facial Pain Clinical Trial
Official title:
Complex Oro-Facial Pain: Functional Imaging Characterization and Treatment With Transcranial Magnetic Stimulation
Verified date | March 2021 |
Source | University of Minnesota |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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: 1. To establish baseline patterns of MRI in patients with chronic oro-facial pain without a definitive etiologic diagnosis. 2. To estimate the rate of treatment success of transcranial stimulation of the primary motor cortex (M1) in these patients. 3. To identify post-treatment MRI patterns that are associated with treatment success.
Status | Completed |
Enrollment | 9 |
Est. completion date | August 30, 2019 |
Est. primary completion date | July 1, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 110 Years |
Eligibility | Inclusion Criteria: - 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 Exclusion Criteria: - 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 |
Country | Name | City | State |
---|---|---|---|
United States | University of Minnesota | Minneapolis | Minnesota |
Lead Sponsor | Collaborator |
---|---|
University of Minnesota |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Young Mania Rating Scale (YMRS) | The Young Mania Rating Scale (YMRS) is one of the most frequently utilized rating scales to assess manic symptoms. The scale has 11 items and is based on the patient's subjective report of his or her clinical condition over the previous 48 hours.
The YMRS total score ranges from 0 to 60 where higher scores indicate more severe mania. |
pre-treatment, 3 and 7 days post treatment | |
Primary | Visual Analogue Scale (VAS) | 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. | 7 days | |
Secondary | World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Overall | A questionnaire used to determine the impact and burden of a disease on daily life. This assessment has 26 questions and covers the domains of physical and psychological health, social relationships, and environment. The answers to various question are included in one or more of the domains. Raw scores are transformed in several different ways by different investigators. We report raw scores. Domains have the following raw score ranges: Overall Quality of Life 2-10, Physical Heath 7-35, Psychological Health 6-30, Social Relationships 3-15, Environment 8-40, Total Raw Score 26-130. Higher scores in each of the domains correspond to greater perceived quality of life. | pre-treatment, 3 and 7 days post treatment | |
Secondary | World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Physical Health | A questionnaire used to determine the impact and burden of a disease on daily life. This assessment has 26 questions and covers the domains of physical and psychological health, social relationships, and environment. The answers to various question are included in one or more of the domains. Raw scores are transformed in several different ways by different investigators. We report raw scores. Domains have the following raw score ranges: Overall Quality of Life 2-10, Physical Heath 7-35, Psychological Health 6-30, Social Relationships 3-15, Environment 8-40, Total Raw Score 26-130. Higher scores in each of the domains correspond to greater perceived quality of life. | baseline, 3 and 7 days post treatment | |
Secondary | World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Psychological Health | A questionnaire used to determine the impact and burden of a disease on daily life. This assessment has 26 questions and covers the domains of physical and psychological health, social relationships, and environment. The answers to various question are included in one or more of the domains. Raw scores are transformed in several different ways by different investigators. We report raw scores. Domains have the following raw score ranges: Overall Quality of Life 2-10, Physical Heath 7-35, Psychological Health 6-30, Social Relationships 3-15, Environment 8-40, Total Raw Score 26-130. Higher scores in each of the domains correspond to greater perceived quality of life. | baseline, 3 and 7 days post treatment | |
Secondary | World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Social Relationships | A questionnaire used to determine the impact and burden of a disease on daily life. This assessment has 26 questions and covers the domains of physical and psychological health, social relationships, and environment. The answers to various question are included in one or more of the domains. Raw scores are transformed in several different ways by different investigators. We report raw scores. Domains have the following raw score ranges: Overall Quality of Life 2-10, Physical Heath 7-35, Psychological Health 6-30, Social Relationships 3-15, Environment 8-40, Total Raw Score 26-130. Higher scores in each of the domains correspond to greater perceived quality of life. | baseline, 3 and 7 days post treatment | |
Secondary | World Health Organization Quality of Life Abbreviated (WHOQOL-BREF) Environment | A questionnaire used to determine the impact and burden of a disease on daily life. This assessment has 26 questions and covers the domains of physical and psychological health, social relationships, and environment. The answers to various question are included in one or more of the domains. Raw scores are transformed in several different ways by different investigators. We report raw scores. Domains have the following raw score ranges: Overall Quality of Life 2-10, Physical Heath 7-35, Psychological Health 6-30, Social Relationships 3-15, Environment 8-40, Total Raw Score 26-130. Higher scores in each of the domains correspond to greater perceived quality of life. | baseline, 3 and 7 days post treatment |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT02957097 -
Gabapentin as a Pre-emptive Analgesic in Oral and Maxillofacial Surgical Procedures
|
Phase 4 | |
Recruiting |
NCT05615714 -
Paresthesia-free Peripheral Nerve Field Stimulation for Trigeminal Neuralgia (FreeST Trial)
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT01554332 -
Motor Cortex Stimulation for Chronic Neuropathic Pain
|
N/A | |
Terminated |
NCT01849796 -
Transcranial Stimulation (tDCS) For the Treatment of Neuropathic Facial Pain
|
Phase 2 | |
Completed |
NCT00462566 -
The Efficacy of Motor Cortex Stimulation for Pain Control
|
N/A | |
Active, not recruiting |
NCT05147454 -
MRI & QST Analysis in Trigeminal Neuralgia and Persistent Idiopathic Facial Pain
|
||
Completed |
NCT04819763 -
Physical Exercises for Temporomandibular Disorders
|
N/A | |
Completed |
NCT03462290 -
Botox Injections for Patients With Persistent Facial Pain
|
Phase 2 | |
Active, not recruiting |
NCT04779476 -
Effectiveness of Alveogyl and Cutanplast Dressing on Postoperative Pain Following Tooth Extraction: A Clinical Trial
|
||
Recruiting |
NCT05479604 -
Treatment of Sinus Headache Using a Novel Device That Combines Acoustic Vibration With Oscillating Expiratory Pressure
|
N/A | |
Active, not recruiting |
NCT02131714 -
Pressure Pain Threshold of Jaw Muscles in TMD Patients Submitted to a Conservative Treatment
|
N/A | |
Completed |
NCT05240703 -
Stabilization Splint Treatment of TMD
|
N/A | |
Terminated |
NCT00122915 -
CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intractable Neuropathic Pain
|
Phase 3 | |
Completed |
NCT00355160 -
Non-Rhinologic Etiologies of Headaches and Facial Pain in Tertiary Care Setting
|
N/A | |
Recruiting |
NCT04467398 -
Incidence of Intravascular (IV) Injection During Trigeminal Nerve Blocks
|
||
Completed |
NCT02021357 -
Proprioceptive Treatment for Temporomandibular Dysfunction
|
N/A | |
Completed |
NCT00008476 -
Capsaicin to Control Pain Following Third Molar Extraction
|
Phase 2 | |
Completed |
NCT03189823 -
Long-term Effect of Motor Cortex Stimulation in Patients Suffering From Chronic Neuropathic Pain
|
N/A | |
Enrolling by invitation |
NCT06299995 -
Phenotype and Burden of a Midfacial Segment Pain
|
||
Completed |
NCT04249427 -
Erenumab for Idiosyncratic Facial Pain
|
Phase 4 |