Deep Brain Stimulation in Patients With Chronic Treatment Resistant Depression (STHYM)

Rennes University Hospital

Status: Completed

Conditions: Major Depressive Disorder; Bipolar Disorder; Recurrent Depressive Disorder

Treatments: Device: SHAM; Device: DBS

Study type: Interventional

Funder types: Other

Identifiers

NCT01973478

35RC08_8902

Details and patient eligibility

About

Major depressive disorders are real public health issues in terms of diagnosis and treatment. Some forms of depression are chronic and resistant to treatment (TRD). In these forms suicide risk is important.

Patients with TRD are potential candidates for neurosurgical interventions to treat depression. However, psychosurgery interventions based upon lesions, showed their limitations related to 1. the large variability in neurosurgical gestures, 2. their side effects, and of course 3. the irreversible damage caused by the surgery.

Thus, deep brain stimulation (DBS) could represent an opportunity for patients suffering from TRD. Our preliminary study based upon the stimulation of the accumbens nucleus showed encouraging results. The investigators have thus planned a randomized controlled trial versus sham stimulation to confirm the therapeutic value of nucleus accumbens DBS.

Full description

Because of their recurrent nature, their prevalence and their consequences, major depressive disorders are real public health issues in terms of diagnosis and treatment.

Some forms of depression are chronic and resistant to treatment (TRD), either unipolar (repeated episodes of depression) or bipolar (repeated episodes of depression and manic and/or hypomanic episodes). In these forms suicide risk is important.

Patients with TRD are potential candidates for neurosurgical interventions to treat depression. The benefit of neurosurgical procedures is expected to be important in these patients.

Psychosurgery interventions based upon lesions, however, showed their limitations related to 1/ the large variability in neurosurgical gestures, 2/ their side effects, and of course 3/ the irreversible damage caused by the surgery.

Current brain imaging data yielded fresh information about the pathophysiology of depression and suggested new therapeutic approaches in TRD.

Modulation of sub-caudate specific pathways, which are part of orbitofrontal and anterior cingulate cortico-subcortical loops should allow for a diminution of depressive symptoms.

The modulation of these specific pathways, initially targeted by classical neurosurgery, could benefit from current developments in functional neurosurgery.

Deep brain stimulation (DBS) may represent an opportunity for patients suffering from TRD. Our preliminary study based upon the stimulation of the accumbens nucleus showed encouraging results. The investigators have thus planned a randomized controlled trial versus sham stimulation to confirm the therapeutic value of nucleus accumbens DBS.

Enrollment: 9 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Age between 18 and 70 years

• DSM-IV (DSM = Diagnostic and Statistical Manual) criteria for a recurrent depressive disorder or bipolar disorder

• Duration of the episode > 2 years

• Severity of the episode attested by :

  • A HDRS score > 21
  • A CGI score ≥ 4
  • A GAF < 50

• Persistence of severity criteria during the screening

• Following characteristics resistance in case of recurrent depressive disorder :

  • Stage V of the classification of Thase and Rush
  • Unsuccessful treatment by the association of two antidepressants (or intolerance/contra-indications)
  • Unsuccessful treatment by the association for at least 6 weeks of one of the following treatments : lithium , thyroid hormone , buspirone , pindolol with an antidepressant (or intolerance/contra-indications)
  • Unsuccessful treatment by the combination of a second-generation antipsychotic (olanzapine, risperidone, amisulpride, aripiprazole, clozapine and quetiapine) to an antidepressant (or intolerance/contra-indications)
  • Unsuccessful treatment by a structured psychotherapy

• Following characteristics of resistance in case of bipolar disorder:

  • Unsuccessful treatment by lithium (or intolerance/contra-indications)
  • Unsuccessful treatment by at least one mood stabilizer anticonvulsant (or intolerance/contra-indications)
  • Unsuccessful treatment by at least one second-generation antipsychotic (or intolerance/contra-indications)
  • Unsuccessful treatment by the combination of two mood stabilizers with at least an anticonvulsant (or intolerance/contra-indications)
  • Unsuccessful treatment by electro-convulsive therapy sessions (or intolerance/contra-indications)
  • Unsuccessful treatment by at least one antidepressant , mood stabilizer combination (or intolerance/contra-indications)
  • Unsuccessful treatment by a structured psychotherapy

• Understanding the conduct of the study

• Giving a written informed consent

• Benefiting from the french social insurance

Non-Inclusion Criteria:

• Comorbid axis 1 disorder (except dysthymia, generalized anxiety disorder, social phobia, panic disorder)
• Alcohol or other psychoactive substances dependence (except nicotine)
• Suicidal risk during the last month assessed by the MINI (Mini International Neuropsychiatric Interview), the DIGS (Diagnostic Interview for Genetic Studies) and the item 3 of the HDRS
• Suicide attempt in the last 6 months or two suicide attempts in the previous two years
• History of forensic act or furious mania
• Depressive episode with congruent or incongruent psychotic features or history of a depressive episode with psychotic features
• Comorbid cluster A or B personality disorders according to the DSM IV-TR evaluated using the SCID2 (Structured Clinical Interview for DSM-IV)
• Cognitive Impairment (Mattis < 130)
• MRI (Magnetic Resonance Imaging) contraindication to stimulation or contraindications for MRI
• Major somatic disease making it impossible to set up the study treatment
• Pregnant women, or nursing or childbearing potential without effective contraception
• Involuntary commitment
• Guardianship
• Participation in another study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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9 participants in 2 patient groups

DBS

Experimental group

Description:

The medical device includes: * Either a pacemaker ACTIVA PC (Ref 37601) two-channel (Medtronic USA) or two pacemakers Activa SC (Ref 37603) to a channel (Medtronic USA) * Two DBS electrodes with four contacts (type Medtronic DBS 3389). Patients will be operated with the usual stereotactic surgical procedure. The target is the Accumbens nucleus. The two electrodes are implanted in a single session under local anaesthesia or intermittent sedation (propofol parenteral without intubation early intervention). Day 0 is defined by the surgery. The DBS is "on" during 6 months (between Month 1 and Month 7). Stimulation will also be on after Month 7.

Treatment:

Device: DBS

SHAM

Sham Comparator group

Description:

The medical device includes: * Either a pacemaker ACTIVA PC (Ref 37601) two-channel (Medtronic USA) or two pacemakers Activa SC (Ref 37603) to a channel (Medtronic USA) * Two DBS electrodes with four contacts (type Medtronic DBS 3389). Patients will be operated with the usual stereotactic surgical procedure. The target is the Accumbens nucleus. The two electrodes are implanted in a single session under local anaesthesia or intermittent sedation (propofol parenteral without intubation early intervention). Day 0 is defined by the surgery. The DBS is "off" during 6 months (between Month 1 and Month 7). Possibility to active the stimulation after Month 7.

Treatment:

Device: SHAM