Viewing Study NCT02422290



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Last Modification Date: 2024-10-26 @ 11:41 AM
Study NCT ID: NCT02422290
Status: COMPLETED
Last Update Posted: 2020-08-17
First Post: 2015-04-13

Brief Title: Ketamine Treatment for Pediatric-Refractory Obsessive-Compulsive Disorder OCD
Sponsor: New York State Psychiatric Institute
Organization: New York State Psychiatric Institute

Study Overview

Official Title: Ketamine Treatment for Pediatric-Refractory Obsessive-Compulsive Disorder OCD
Status: COMPLETED
Status Verified Date: 2020-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This pilot study is proposed to determine the acceptability feasibility and potential efficacy of ketamine a medication that modulates glutamate in the brain as a rapid treatment for obsessive-compulsive disorder OCD symptoms in adolescents and young adults with OCD This study will recruit 6 youth ages 14-22 who are diagnosed with clinically significant OCD and have failed at least one adequate trial of a Serotonin Reuptake Inhibitor SRI medication and a course of Cognitive-Behavioral Therapy CBT unless unable to access or tolerate for OCD in the past Participants will receive a single infusion of intravenous ketamine and be assessed at regular intervals post-infusion for up to 14 days At the end of the 14-day treatment phase all participants will be offered three months of open treatment for OCD with medication andor CBT
Detailed Description: See Brief Summary for description

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None