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Device

Deep Brain Stimulation for Autism

N/A
Waitlist Available
Led By George Ibrahim, MD
Research Sponsored by The Hospital for Sick Children
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights

Summary

This trial tests a device that sends electrical signals to the brain to help children with autism who hurt themselves and don't get better with usual treatments. The device aims to calm the brain areas causing these behaviors. This method has shown promise in treating autism by improving behavior.

Who is the study for?
This trial is for children aged 7-18 with Autism Spectrum Disorder who engage in repetitive self-harm and haven't improved after at least 6 months of medical therapy. Participants must have a caregiver able to consent and commit to all study requirements for one year. Exclusions include pregnancy, inability to complete questionnaires in English, potential relocation, certain health risks from surgery, and recent substance abuse.
What is being tested?
The trial tests the safety and potential effectiveness of Deep Brain Stimulation (DBS) on the nucleus accumbens in children with autism who self-harm despite treatment. Six patients will receive surgical implantation of the Medtronic DBS system over a one-year pilot phase I trial without blinding or randomization.
What are the potential side effects?
Potential side effects may include those associated with brain surgery such as infection risk, bleeding, headache or discomfort at the electrode site; stimulation-related effects like mood changes or seizures; plus device-specific issues like malfunction.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Changes in abberant behaviour
Changes in obsessive-compulsive thoughts
Changes in quality of life
+2 more
Secondary study objectives
Changes in activity
Changes in metabolic brain abnormalities
Changes in physical brain abnormalities

Side effects data

From 2018 Phase 2 trial • 53 Patients • NCT01221948
23%
Fall
15%
Depression
8%
Hand fracture
8%
Restless legs syndrome
8%
Apathy
5%
Skeletal injury
5%
Dyspepsia
5%
Back pain
5%
Head injury
5%
Speech disorder
5%
Tremor
5%
Gait disturbance
5%
Dystonia
5%
Paraesthesia
5%
Influenza
5%
Urinary tract infection
3%
Contusion
3%
Alcohol poisoning
3%
Hypoaesthesia
3%
Diplopia
3%
Joint sprain
3%
Macular degeneration
3%
Fluid retention
3%
Device migration
3%
Skin laceration
3%
Akinesia
3%
Parkinson's disease
3%
Syncope
3%
Respiratory depression
3%
Productive cough
3%
Diabetes mellitus
3%
Ingrowing nail
3%
Postoperative wound infection
3%
Intervertebral disc protrusion
3%
Osteoarthritis
3%
Pain in extremity
3%
Spinal osteoarthritis
3%
Rib fracture
3%
Drug withdrawal syndrome
3%
Cerebral microangiopathy
3%
Dysarthria
3%
Memory impairment
3%
Movement disorder
3%
Monarthritis
3%
Neck pain
3%
Adverse drug reaction
3%
Cyst
3%
Implant site haematoma
3%
Oedema peripheral
3%
Pyrexia
3%
Pleural effusion
3%
Nerve root lesion
3%
Anxiety
3%
Cough
3%
Fibula fracture
3%
Thermal burn
3%
Sciatica
3%
Anger
3%
Bursitis
3%
Cystitis
3%
Helicobacter gastritis
3%
Implant site infection
3%
Localised infection
3%
Pneumonia
3%
Staphylococcal infection
3%
Confusional state
3%
Depressed mood
3%
Hallucination, auditory
3%
Impulse-control disorder
3%
Insomnia
3%
Panic attack
3%
Rapid eye movements sleep abnormal
3%
Bronchitis
3%
Ear infection
3%
Incision site infection
3%
Arthralgia
3%
Axillary pain
3%
Folate deficiency
3%
Hypertension
3%
Hypotension
3%
Thrombophlebitis
3%
Laboratory test abnormal
3%
Weight increased
3%
Pericardial effusion
3%
Seborrhoeic keratosis
3%
Urinary incontinence
100%
80%
60%
40%
20%
0%
Study treatment Arm
Deep Brain Stimulation

Trial Design

1Treatment groups
Experimental Treatment
Group I: DBS TreatmentExperimental Treatment2 Interventions
Deep brain stimulation of both limbic and dysfunctional reward processing circuits for treatment of repetitive self injurious behaviours in children with ASD
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Deep Brain Stimulation
2011
Completed Phase 2
~710
DBS
2011
Completed Phase 1
~40

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Autism Spectrum Disorder (ASD) include behavioral and educational interventions, which focus on modifying behavior through reinforcement techniques and structured learning environments. Deep Brain Stimulation (DBS), specifically targeting the nucleus accumbens, modulates neural activity by delivering electrical impulses to specific brain regions involved in behavior and reward processing. This can potentially reduce severe repetitive behaviors and self-injury in treatment-refractory cases. Understanding these mechanisms is crucial as they directly influence the neural circuits associated with core ASD symptoms, offering targeted and potentially more effective therapeutic options for patients who do not respond to conventional treatments.
Modulation of Resting-State Brain Complexity After Bilateral Cerebellar Anodal Transcranial Direct Current Stimulation in Children with Autism Spectrum Disorders: a Randomized Controlled Trial Study.

Find a Location

Who is running the clinical trial?

The Hospital for Sick ChildrenLead Sponsor
704 Previous Clinical Trials
6,956,871 Total Patients Enrolled
George Ibrahim, MDPrincipal InvestigatorThe Hospital for Sick Children

Media Library

DBS (Device) Clinical Trial Eligibility Overview. Trial Name: NCT03982888 — N/A
Autism Research Study Groups: DBS Treatment
Autism Clinical Trial 2023: DBS Highlights & Side Effects. Trial Name: NCT03982888 — N/A
DBS (Device) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03982888 — N/A
~1 spots leftby Sep 2025