Glucose Consumption During Deep Brain Stimulation With Functional [18F]FDG-Brain-PET in Obsessive-Compulsive Disorder
Run by Medical University of Vienna · NCT05577598 · Data updated 2026-11-12
This study is testing how the brain uses sugar during deep brain stimulation to see if it helps people with obsessive-compulsive disorder.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 8 (estimated) |
| Sponsor | Medical University of Vienna Academic / other |
| Locations | 1 site (Vienna, State of Vienna) |
| Status | Recruiting |
| Started | April 1, 2022 |
| Main results expected | May 1, 2026 |
| Study ends | September 1, 2026 |
| Registry record updated | June 13, 2025 |
| Trial ID | NCT05577598 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Unknown
✕Probably not a fit
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A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
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Why it matters
Potential benefit: Unknown
How similar studies have gone: Unknown
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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, if tolerated, beyond the FDA maximum recommended dose for a minimum duration over at least ten weeks each. * at least one trial with tricyclic medication at or, if tolerated, beyond the FDA maximum recommended dose for a minimum duration over at least ten weeks each. * at least one trial of augmentation with antipsychotic medication, lithium, a benzodiazepine or buspirone * at least on trial of psychotherapy (cognitive behavioral therapy or comparable techniques) for at least 20 sessions * ability to provide written informed consent Exclusion Criteria: * any history of current or past psychotic disorder * a manic episode within the preceding three years * any current clinically significant medical or neurological disorder, that is a contraindication against DBS * any disease that could lead to an 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 duration (desire to have children) and refusal to utilize a proper method of 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
Where it's running
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Medical University of Vienna, Department of Psychiatry and Psychotherapy
Vienna, State of Vienna, Austria Recruiting
Study contacts
- Principal investigator: Christoph Kraus, MD PhD — Medical University of Vienna, Department of Psychiatry and Psychotherapy
- Study coordinator: Christoph Kraus, MD PhD
- Email: christoph.kraus@muv.ac.at
- Phone: +43 1 40400 73882
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.