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Deep Brain Stimulation of NAc/ALIC to Prevent Treatment-Refractory Obsessive Compulsive Disorder

Deep Brain Stimulation of Nucleus Accumbens/Anterior Limb of Internal Capsule to Prevent Treatment-Refractory Obsessive Compulsive Disorder

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02601677
Enrollment
10
Registered
2015-11-10
Start date
2015-11-30
Completion date
2018-11-30
Last updated
2015-11-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obsessive Compulsive Disorder

Keywords

Obsessive Compulsive Disorder, Deep Brain Stimulation, Nucleus accumbens

Brief summary

Nucleus accumbens/anterior limb of internal capsule play important roles in the process of treatment-refractory obsessive compulsive disorder, deep brain stimulation of nucleus accumbens/anterior limb of internal capsule will inhibit its activity and thus to effectively prevent the disorder.

Detailed description

Obsessive-compulsive disorder (OCD) is characterized by obsessions (persistent thoughts) and compulsions (repetitive ritualistic behaviour). Core symptoms of OCD cause remarkable distress and often perceived as inappropriate. The prevalence of OCD in the general population is estimated between 1% and 3%. It is a psychiatric illness that can lead to chronic functional impairment. Treatment options for OCD include cognitive behavioural therapy (CBT) and/or pharmacotherapy. Even when the best treatment options are used, approximately 10% of these patients remain severely affected and are considered therapy-refractory resulting in marked suffering and impairment in self-care, work and social life. More recently, deep brain stimulation (DBS) has been investigated as a therapy for refractory OCD, and the procedure was granted a limited humanitarian device exemption by the FDA in 2009. For these patients, deep brain stimulation (DBS), a neurosurgical treatment that involves stereotactic implantation of electrodes in specific deep-seated brain regions, has emerged as a new treatment option.

Interventions

PROCEDUREDeep brain stimulation

Deep brain stimulation of bilateral Nucleus accumbens/Anterior Limb of Internal Capsule

DRUGFluoxetine

Fluoxetine is one of selective serotonin reuptake inhibitors(SSRIs).

Sponsors

Tang-Du Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. Diagnosis of OCD following the diagnostic and statistical manual of mental disorders-fourth edition (DSM-IV) criteria for OCD; 2. Duration of illness: min. 5 year; 3. 18 years old \<Age \<60 years old; 4. Severe form of OCD, as evidenced by: a score≥25 on the Y-BOCS, a score \> 4 on the CGI scale, a score≤40 on the GAF (global assessment of functioning). 5. All patients were lack of response to drug therapy after adequate administration (defined as more than 12 weeks at the maximum tolerated dose) of at least four different medications, lack of response to CBT (Cognitive Behaviour Therapy)over the course of 1 year of therapy or after 20 sessions. 6. Normal cognitive status and ability to understand and comply with instructions for multiple therapies. 7. Good overall health.

Exclusion criteria

1. Present or past history of psychotic symptoms. 2. Severe personality disorders; 3. Any clinically significant neurological disorder or medical illnesses affect ; 4. brain function, other than motor tics or Gilles de la Tourette syndrome; 5. Patient currently treated with anticoagulant or antiplatelet drug; 6. Patient with contraindication for surgery or anesthesia; 7. Inability to undergo awaked operation; 8. Infection, coagulopathy, significant cardiac or other medical risk factors for surgery; 9. Patient with contraindication for MRI scanning (cardiac pacemaker, pregnancy, metal in body, severe claustrophobia), abnormal brain MRI or serious inter current disease

Design outcomes

Primary

MeasureTime frame
Yale-Brown Obsessive Compulsive Scale (Y-BOCS)6 month

Secondary

MeasureTime frame
Global assessment of functioning (GAF)6 month
The Hamilton Anxiety Scale (HAM-A)6 month
The Hamilton Rating Scale for Depression (HAM-D)6 month
Clinical Global Impression (CGI)6 month
Event related potentials(ERPs)Baseline,3 month,6 month and 12 month
local field potential(LFP)in surgery,7 days after surgery
Change in two static positron emission tomography(PET) images studyBaseline and 6month follow-up
Sheehan Disability Scale (SDS)6 month

Contacts

Primary ContactGuo-dong Gao, M.D.
gguodong@fmmu.edu.cn+86 29 84777435
Backup ContactXue-lian Wang, M.D.
wxlian@fmmu.edu.cn+86 29 84777284

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026