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Clinical Trial Summary

The main goal of this trial is to demonstrate therapeutic efficacy of low dose ketamine in patients with OCD. We expect that ketamine will alleviate symptoms in the hours following application, but also - if effective - that the anti-OCD effects might last for several days after a single infusion.


Clinical Trial Description

This study will apply a randomized, double blind, comparator-controlled cross-over design and will be conducted at the Department of Psychiatry and Psychotherapy of the Medical University of Vienna. We will include 30 participants with a primary diagnosis of OCD. Participants will undergo ketamine and comparator infusions in either inpatient- or outpatient settings to assess the therapeutic capabilities of ketamine in OCD. Furthermore, participants' neurocognitive function and stress responses will be tested with four neurocognitive tasks and a cold pressor test paradigm. Study subjects will be given an option to participate in an open-label follow up with up to 8 infusions over a period of a month. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05577585
Study type Interventional
Source Medical University of Vienna
Contact Christoph Kraus, MD PhD
Phone +4314040035680
Email christoph.kraus@muv.ac.at
Status Recruiting
Phase N/A
Start date October 1, 2022
Completion date June 2026

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