Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
NCT02377375

Deep Brain Stimulation (DBS) for Obsessive Compulsive Disorder (OCD): Improving Targeting Precision

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-07-10

10

Participants Needed

1

Research Sites

569 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

When comparing targeting precision between DBS in parkinsonian patients and OCD patients, an unexpected deviation from the planned targets was discovered in OCD patients (Nuttin et al., 2013). The objective of this trial is to investigate whether the use of a micro-electrode assisted technique improves targeting precision in DBS at the BNST.

CONDITIONS

Official Title

Deep Brain Stimulation (DBS) for Obsessive Compulsive Disorder (OCD): Improving Targeting Precision

Who Can Participate

Age: 20Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of OCD following DSM-IV criteria (300.3)
  • Documented failure of pharmacotherapy trials following OCD treatment guidelines
  • Documented failure of cognitive and behavioral therapy
  • Duration of illness of at least 5 years
  • Yale-Brown Obsessive Compulsive Scale (Y-BOCS) score of at least 30 out of 40
  • Age between 20 and 65 years
Not Eligible

You will not qualify if you...

  • Severe personality disorder in cluster A or B with high risk for acting-out behavior
  • Organic brain pathology or significant abnormalities on MRI
  • Present or past history of psychotic symptoms
  • Current substance abuse or unstable remission within the last 12 months
  • Any disorder affecting cognitive function other than motor tics or Gilles de la Tourette's Syndrome
  • Mental retardation preventing adequate questionnaire reporting and instrument handling

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

UZ Leuven

Leuven, Vlaams-Brabant, Belgium, 3000

Actively Recruiting

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Research Team

B

Bart Nuttin, MD, PHD

CONTACT

S

Simon Raymaekers, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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