Trial Search Results
Sphenopalatine Ganglion Stimulation for the Treatment of Chronic Cluster Headache
The primary objective of the study is to demonstrate the safety and efficacy of SPG stimulation with the ATI Neurostimulation System when used to treat acute cluster attacks in chronic cluster headache patients.
Stanford is currently not accepting patients for this trial.
Autonomic Technologies, Inc.
- Device: ATI Neurostimulation System
- Age from ≥22 years old.
- Subject has been diagnosed with chronic cluster headache according to the 2013 ICHD,
3rd edition (beta version), criterion 3.1.2.
- Subject reports a minimum of 4 cluster attacks per week on the side of their dominant
headache laterality. Subjects who report more than 8 attacks per day or attack
duration of less than 30 minutes (untreated or unsuccessfully treated) must have been
tested to rule out other forms of trigeminal autonomic cephalalgias.
- Both subject and physician judge previously or currently used preventive and/or acute
cluster headache treatment to be inadequate.
- Subject is able to distinguish cluster attacks from other headaches (i.e., migraine,
- Subject agrees to not use therapy involving TENS or magnetic field treatment while the
Neurostimulator is implanted.
- Subject agrees to not participate in supplemental or alternative therapy, including
acupuncture and spinal manipulation, from Study Enrollment through the end of the
Experimental Period of the study.
- Subject agrees to maintain current preventive headache medication regimens (no change
in type, frequency, or dose) - except to manage tolerability - from Study Enrollment
through the Experimental Period of the study.
- Subject agrees not to use any acute medications, including oxygen therapy, for their
treatable cluster attacks during the Experimental Period until after they have used
SPG stimulation therapy for at least 15 minutes.
- Subject has had a dental examination and cleaning in the past six (6) months.
- Subject has the ability to read and comprehend, and to reliably record information as
required by the Protocol.
- Subject is able to provide written informed consent prior to participation in the
- Subject's overall health, age and/or comorbidities place subject at high risk for
complications from surgery and/or general anesthesia.
- Subject has had a change in type, dosage or dose frequency of preventive headache
medications < one (1) month prior to study enrollment
- Subject has been diagnosed with any other form of Trigeminal Autonomic Cephalalgias
(e.g., paroxysmal hemicrania, SUNCT, etc.) or has a history of trigeminal neuralgia.
- Subject has undergone facial surgery in the area of the pterygopalatine fossa or
zygomaticomaxillary buttress ipsilateral to the planned implant site that, in the
opinion of the Investigator, may lead to an inability to properly implant the
- Subject currently has an active oral or dental abscess or an active maxillary sinus
infection based on present symptoms.
- Subject has been treated with therapeutic radiation to the facial region.
- Subject has been diagnosed with any major infectious processes such as osteomyelitis,
or primary or secondary malignancies involving the face that have been active or
required treatment in the past six (6) months.
- Subject has other significant pain problem(s) that, in the opinion of the
Investigator, might confound the study assessments.
- Subject is a woman of childbearing potential who is pregnant, nursing, or not using
- Subject is currently participating or has participated in the last month in another
clinical study in which the subject has, is, or will be exposed to an investigational
or non-investigational drug or device.
- Subject has demonstrated or is believed to be at risk of non-compliance with study
procedures (e.g., for completing the diary or maintaining a stable headache medicine
regimen or returning for required follow-up visits).
- Subject is at risk of being unable to complete at least 1 year of follow-up (e.g., has
plans to relocate).
- Subject has had previous lesional radio-frequency (RF) ablation, balloon compression,
gamma knife, or glycerol treatments of the ipsilateral sphenopalatine ganglion (SPG),
trigeminal ganglion or any branch of the trigeminal nerve.
- Subject has had blocks or non-lesional pulsed RF of the ipsilateral SPG in the last
three (3) months.
- Subject's pterygomaxillary fissure is less than 1.2 mm in width at the level of the
vidian canal, as determined by CT scan.
- Subject has undergone onabotulinumtoxinA injections of the head and/or neck or has had
an occipital nerve block in the last three (3) months.
- Subject has or requires an active implanted medical device, such as a
pacemaker/defibrillator, other neurostimulator, or cochlear implant.
- Subject is expected to require diathermy, electroconvulsive therapy (ECT), or
transcranial magnetic stimulation (TMS).
- Subject has a history of bleeding disorders or coagulopathy and is unable to
discontinue anticoagulation, antiplatelet, or GP IIb IIIa inhibitor medication in
preparation for the implantation procedure.
- In the opinion of the Investigator, the subject currently meets criteria as defined by
the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) for an active
major depressive episode or for active significant psychiatric disorders, including
dementia, uncontrolled general anxiety disorder, psychotic disorders or uncontrolled
bipolar disorder. Exclusion criteria also include: active psychosis, untreated severe
anxiety disorder, homicidal ideation, significant Axis II disorders and significant
untreated sleep disorders.
- Subject currently has clinically significant drug or alcohol abuse as defined by
DSM-IV-TR or is unable to refrain from substance abuse throughout the study.
- Subject has a history of malignancy or any other condition that requires MRI
- Subject has a history of allergic or hypersensitive reactions to titanium, platinum,
or implant grade silicone-polyurethane copolymers.
- Subject may be, in the opinion of the Investigator, at greater risk of infection
(e.g., subjects with diabetes, taking steroids, with gingivitis/periodontitis,
malnutrition or anorexia/bulimia) or at higher risk of harm from infections.
- Subject is currently using a tobacco cessation regimen (e.g. Wellbutrin, Zyban,
- Subject is not suitable for the study for any reason (including overall health,
pre-existing conditions or medications) in the judgment of the Investigator.
Ages Eligible for Study
22 Years - N/A
Genders Eligible for Study