Obsessive-Compulsive Disorder Clinical Trial
Official title:
Adjunct Cortical Stimulation With Deep Brain Stimulation (DBS) to Treat Obsessive Compulsive Disorder (OCD)
NCT number | NCT04958096 |
Other study ID # | 21-33743 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | August 1, 2021 |
Est. completion date | August 1, 2026 |
The purpose of this study is to identify abnormal brain signals associated with Obsessive Compulsive Disorder (OCD) and psychiatric symptoms and to investigate novel therapeutic stimulation sites. While treating OCD with standard deep brain stimulation (DBS) therapy, the investigators will also monitor the activity of the anterior cingulate and prefrontal cortex, a region known be involved with OCD, decision making, and emotion regulation, and the investigators will identify abnormal activity corresponding to the severity of a patient's OCD. The investigators will also investigate whether it is possible for stimulation delivered to these parts of the brain can improve OCD symptoms. These investigations have the potential to aid in the development of improved forms of DBS that can better target abnormal OCD brain signatures in the future. The investigators will implant a cortical electrode in addition to the ALIC DBS electrode and connect these to an implantable pulse generator that care store field potential data (Medtronic Percept). The decision whether the lead is placed in the prefrontal or cingulate cortex bilaterally will be based upon considerations of the surgical risks for a particular patient based upon their anatomy and the required surgical approach. At multiple time points post-implantation up to 2 years, in our clinic or patient's homes, cortical and subcortical signals will be recorded. Data will be collected while patient are resting or engaged in symptom provocation tasks, emotional/cognitive tasks while cortical stimulation is on and off. In addition to brain signal recordings, symptoms will be assessed using validated questionnaires and tasks to allow identification of neurophysiological correlates of OCD symptoms.
Status | Recruiting |
Enrollment | 15 |
Est. completion date | August 1, 2026 |
Est. primary completion date | August 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 22 Years to 75 Years |
Eligibility | Inclusion Criteria: - Ability to give informed consent for the study - Age 22-75 - Clinical diagnosis of OCD - Documented duration of OCD of at least 5 years - OCD rated as severe or extreme illness (YBOCs = 28) - Has failed to improve following treatment with at least two selective serotonin reuptake inhibitors (SSRIs), clomipramine, and augmentation with antipsychotics - Has not responded to adequate trials of cognitive behavior therapy (exposure and response prevention) - Has not responded adequately to TMS treatment for OCD if it is reasonably available to the patient Exclusion Criteria: - Has hoarding as a primary subclassification of OCD according to DSM-4 - Has another severe psychiatric disorder (personality disorder, psychotic/bipolar disorder, etc) or substance abuse issues - Is pregnant - Has an abnormal MRI assessed by the team or has a neurological condition requiring an MRI in the future - Has a cognitive disorder or dementia - Is at imminent risk for suicide based upon Suicide Severity Rating Scale (SSRS) or has ever attempted suicide - Inability to comply with study follow-up visits - Major comorbidity increasing the risk of surgery (prior stroke, severe hypertension, severe diabetes, or need for chronic anticoagulation other than aspirin) - Allergies or known hypersensitivity to materials in the Activa systems (i.e. titanium, polyurethane, silicone, polyethermide, stainless steel). - Previous cranial ablative or deep brain stimulation surgery. - Patients may be excluded from enrollment due to a condition that, in the judgement of the PI, significantly increases risk or reduces significantly the likelihood of benefit from DBS. |
Country | Name | City | State |
---|---|---|---|
United States | UCSF Nancy Friend Pritzker Psychiatry Building | San Francisco | California |
Lead Sponsor | Collaborator |
---|---|
Andrew Moses Lee, MD, PhD |
United States,
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Biomarker identification in Stage 1 | The number of patients in whom we can identify a neural biomarker that accounts for a significant amount of variance in OCD symptom severity | 1-12 months | |
Primary | Change in Yale-Brown Obsessive Compulsive Scale (Y-BOCS) from 12 months to 24 months | The Y-BOCS is an OCD symptom scale used for identifying current OCD symptom severity. The score ranges from 0-40, with higher scores indicating more severe OCD symptoms. The change in Y-BOCS score from 12 months to 24 months will be reported. | 12-24 months | |
Secondary | Change in Montgomery Asberg Depression Rating Scale (MADRS) score from 12 months to 24 months | Effect size of cortical stim + ALIC DBS compared to ALIC DBS (mean difference in Montgomery Asberg Depression Rating Scale (MADRS) score at 12 months and 24 months. Higher MADRS score indicates more severe depression; the overall score ranges from 0 to 60. | 12-24 months |
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