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Clinical Trial Summary

The study will test the efficacy of propranolol or placebo, administered after reactivation of a previously acquired obsessive-compulsive disorder (OCD) fear, in reducing fear and avoidance in OCD.


Clinical Trial Description

Twenty subjects with OCD will be enrolled in the study. Participants will complete baseline assessments of fear and avoidance. Participants will be randomly assigned to a single dose of propranolol 40mg or placebo, administered immediately after a fear reactivation procedure. Primary outcome assessment will be OCD symptoms and avoidance behavior in a behavioral avoidance task 2 weeks after the intervention ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02790710
Study type Interventional
Source New York State Psychiatric Institute
Contact
Status Withdrawn
Phase Phase 4
Start date June 2016
Completion date April 2023

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