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Trial record 2 of 6 for:    Ketamine stanford

Understanding How Ketamine Brings About Rapid Improvement in OCD

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02624596
Recruitment Status : Recruiting
First Posted : December 8, 2015
Last Update Posted : December 12, 2017
Sponsor:
Collaborator:
Information provided by (Responsible Party):

Study Description
Brief Summary:
The purpose of this study is to understand how ketamine brings about rapid improvement in Obsessive-Compulsive Disorder (OCD) symptoms.

Condition or disease Intervention/treatment Phase
Obsessive-Compulsive Disorder Drug: Ketamine Drug: Midazolam Phase 2

Detailed Description:
Obsessive-Compulsive Disorder (OCD) is a chronic and disabling disorder that costs the economy over $2 billion annually and represents a significant public health problem. This study aims to build on our discovery that a potent NMDA receptor antagonist, ketamine, has rapid (in hours) and robust therapeutic effects in OCD. The proposed projects test the acute mechanism of action of ketamine at the level of molecules, circuits, and network synchrony to determine how NMDA receptor antagonism modifies the underlying pathology of OCD to relieve repetitive thoughts and behaviors.

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 120 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: NMDAR Modulation As a Therapeutic Target and Probe of Neural Dysfunction in OCD
Study Start Date : June 2016
Estimated Primary Completion Date : June 2020
Estimated Study Completion Date : June 2021

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Arms and Interventions

Arm Intervention/treatment
Experimental: Ketamine
OCD patients in this arm will receive 0.5mg/kg of ketamine - one single infusion
Drug: Ketamine
OCD patients in this arm will receive 0.5mg/kg of ketamine - one single infusion
Other Name: Ketamine Hydrochloride
Active Comparator: Midazolam
OCD patients in this arm will receive 0.045mg/kg of midazolam - one single infusion
Drug: Midazolam
OCD patients in this arm will receive 0.045mg/kg of midazolam - one single infusion
Other Name: Midazolam Hydrochloride


Outcome Measures

Primary Outcome Measures :
  1. improvement in the severity of OCD symptoms as measured by the Yale-Brown Obsessive Compulsive Scale (YBOCS) [ Time Frame: Up to 6 months ]

Secondary Outcome Measures :
  1. regional gamma-aminobutyric acid, glutamate/glutamine levels derived from 3T Magnetic Resonance Spectroscopy [ Time Frame: up to 90 minutes ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria for participants with OCD:

  • age 18-65
  • Primary diagnosis of OCD
  • Sufficient severity of OCD symptoms
  • ability to tolerate a treatment-free period
  • capacity to provide informed consent

Inclusion criteria for healthy controls:

  • ages 18-65
  • capacity to provide informed consent

Exclusion criteria for participants with OCD:

  • Psychiatric or medical conditions that make participation unsafe
  • pregnant or nursing females
  • concurrent use of any medications that might increase the risk of participation (e.g. drug interactions)
  • presence of metallic device or dental braces

Exclusion criteria for healthy controls:

  • any current or lifetime psychiatric diagnosis
  • pregnant or nursing females
  • major medical or neurological problem
  • presence of metallic device or dental braces
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02624596


Contacts
Contact: Jordan Wilson 650-723-4095 ocdresearch@stanford.edu
Contact: Maria Filippou, MD, MBS 650-723-4095 ocdresearch@stanford.edu

Locations
United States, California
Stanford University Recruiting
Stanford, California, United States, 94305
Contact: Andrea Varias, MSHS    650-723-4095    ocdresearch@stanford.edu   
Contact: Maria Filippou-Frye, MD, MBS    650-723-4095    ocdresearch@stanford.edu   
Principal Investigator: Carolyn Rodriguez, MD, PhD         
Sponsors and Collaborators
Stanford University
University of Connecticut
More Information

Additional Information:
Responsible Party: Carolyn Rodriguez, Principal Investigator, Stanford University
ClinicalTrials.gov Identifier: NCT02624596     History of Changes
Other Study ID Numbers: IRB-34622
First Posted: December 8, 2015    Key Record Dates
Last Update Posted: December 12, 2017
Last Verified: December 2017

Keywords provided by Carolyn Rodriguez, Stanford University:
OCD

Additional relevant MeSH terms:
Ketamine
Compulsive Personality Disorder
Obsessive-Compulsive Disorder
Personality Disorders
Mental Disorders
Anxiety Disorders
Midazolam
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anesthetics, Dissociative
Anesthetics, Intravenous
Anesthetics, General
Anesthetics
Central Nervous System Depressants
Excitatory Amino Acid Antagonists
Excitatory Amino Acid Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Adjuvants, Anesthesia
Hypnotics and Sedatives
Anti-Anxiety Agents
Tranquilizing Agents
Psychotropic Drugs
GABA Modulators
GABA Agents