Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT05577598

Glucose Consumption During Deep Brain Stimulation With Functional [18F]FDG-Brain-PET in Obsessive-Compulsive Disorder

Led by Medical University of Vienna · Updated on 2025-06-13

8

Participants Needed

1

Research Sites

230 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this randomized, sham-controlled study is to evaluate the effectiveness of DBS therapy in individuals suffering from severe OCD and to investigate DBS treatment with functional \[18F\]FDG-Brain-PET.

CONDITIONS

Official Title

Glucose Consumption During Deep Brain Stimulation With Functional [18F]FDG-Brain-PET in Obsessive-Compulsive Disorder

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • A score of 25 or higher on the Yale-Brown Obsessive Compulsive Scale
  • Previous failure to respond to at least two medication trials with serotonin reuptake inhibitors at or beyond FDA maximum recommended dose for at least ten weeks each
  • At least one trial with tricyclic medication at or beyond FDA maximum recommended dose for at least ten weeks
  • At least one trial of augmentation with antipsychotic medication, lithium, a benzodiazepine, or buspirone
  • At least one trial of psychotherapy (cognitive behavioral therapy or comparable techniques) for at least 20 sessions
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Any history of current or past psychotic disorder
  • A manic episode within the preceding three years
  • Any current clinically significant medical or neurological disorder contraindicating DBS
  • Any disease leading to altered glucose reactivity (e.g., diabetes)
  • Any clinically significant preoperative MRI abnormality or inability to undergo presurgical MRI
  • Current or unstable remitted substance abuse or dependence except nicotine
  • Pregnancy or high risk of becoming pregnant during study and refusal to use proper contraception
  • Any current severe personality disorder except comorbid anankastic personality disorder
  • Inability to follow the study protocol or adhere to operational requirements
  • Current and unstable suicidality

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University of Vienna, Department of Psychiatry and Psychotherapy

Vienna, State of Vienna, Austria, 1090

Actively Recruiting

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Research Team

C

Christoph Kraus, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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