Trial intelligence / Profile preview

Intranasal Ketamine for OCD

NCT02234011Phase 2

Key facts

Status
Terminated
Start
Sep 2014
Primary completion
Jan 2016
Countries
1
Sponsor
McLean Hospital
Modality
Small Molecules
Conditions
obsessive compulsive disorder (OCD)
01

Overview

Phase 2, randomised, double-blind trial of ketamine in obsessive compulsive disorder (OCD) (2 arms), sponsored by McLean Hospital. Primary endpoint: Decrease in OCD Symptoms at 5 weeks. Started Sep 2014; status: terminated.

02

Design

2 arms
Study design
RandomizedDouble-blind
  • Ketamine/Placebo

    Ketamine at Visit 1, Placebo at Visit 2

  • Placebo/Ketamine

    Placebo at Visit 1, Ketamine at Visit 2

03

Who it enrols

Adults aged 18-55 with a primary diagnosis of OCD and a Y-BOCS score >= 18. Excludes patients with active suicidal ideation, history of psychotic or autism spectrum disorders, substance dependence, or significant medical/neurologic disease.

04

Endpoints

Primary

  • Decrease in OCD Symptoms

Beyond the preview

Go deeper on NCT02234011.

Full results, competitive context and analysis are in the Gosset platform.

Full results & analysis

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on NCT02234011.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call