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Clinical Trial Summary

The proposed randomized, double-blind research study will use functional magnetic resonance neuroimaging using state-of-the-art HCP acquisition protocols and analytic pipelines, to identify predictors and correlates of response to an accepted first-line pharmacological treatment for obsessive-compulsive disorder.


Clinical Trial Description

The proposed study intends to recruit 2 groups: 1. Matched healthy control participants will be imaged with one fMRI at baseline as a no-treatment comparison group; and 2. a randomized, double-blind group of unmedicated OCD participants who will be assigned to begin either immediate or placebo-delayed treatment, and who will be imaged with fMRIs at baseline and over the course of treatment with a selective serotonin reuptake inhibitor (SSRI), fluoxetine. Hypothesis-driven analyses and exploratory analyses will be performed in parallel. This study will address the following Specific Aims: 1. Identification of neural dysconnectivity associated with OCD symptomatology. 2. Characterizing neural markers of clinical response to SSRI pharmacotherapy. 3. Mapping neural predictors of clinical response to pharmacotherapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04131829
Study type Interventional
Source Yale University
Contact Yale OCD Research Clinic
Phone 1-855-623-9253
Email ocd.research@yale.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date October 14, 2019
Completion date July 31, 2024

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