Pilot Study of Ketamine in Adults With Obsessive-Compulsive Disorder (OCD)
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ClinicalTrials.gov Identifier: NCT01100255 |
Recruitment Status :
Completed
First Posted : April 8, 2010
Results First Posted : October 27, 2016
Last Update Posted : February 20, 2017
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Obsessive-Compulsive Disorder | Drug: Ketamine infusion Other: Saline | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 15 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Masking: | Double (Participant, Investigator) |
Official Title: | Understanding the Glutamate System in Adults With Obsessive-Compulsive Disorder With N-methyl-D Aspartate Antagonist Ketamine |
Study Start Date : | April 2010 |
Actual Primary Completion Date : | December 2015 |
Actual Study Completion Date : | December 2015 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Group A
0.5mg/kg IV ketamine infusion over 40 minutes then IV saline infusion over 40 minutes
|
Drug: Ketamine infusion
0.5mg/kg IV over 40 minutes
Other Name: Ketamine hydrochloride Other: Saline saline infusion |
Active Comparator: Group B
IV saline infusion over 40 minutes then 0.5mg/kg IV ketamine infusion over 40 minutes
|
Drug: Ketamine infusion
0.5mg/kg IV over 40 minutes
Other Name: Ketamine hydrochloride Other: Saline saline infusion |
- Number of Patients Who Met and Exceeded Response Criteria of Yale-Brown Obsessive-Compulsive Scale. [ Time Frame: 1 week ]Patients given YBOCS (Yale Brown Obsessive-Compulsive Scale), a gold standard measure of obsessions and compulsions. For the YBOCS the minimum units are 0 and Maximum units on the total scale are 40. The higher the number on the YBOCS, the more severe the symptoms. Response was defined as at least a 35% reduction on the YBOCS.

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Ages Eligible for Study: | 18 Years to 55 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age 18-55
- Physically healthy and not currently pregnant
- Primary Diagnosis of OCD
- Sufficient severity of symptoms
- Able to provide consent
Exclusion Criteria:
- Psychiatric conditions that make participation unsafe
- Currently on psychotropic medication
- Medical conditions that make participation unsafe
- Allergy to ketamine
- Any metal in the body

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): NCT01100255
United States, New York | |
New York State Psychiatric Institute | |
New York, New York, United States, 10032 |
Principal Investigator: | Carolyn I. Rodriguez, M.D., Ph.D. | Columbia-NYSPI-RFMH |
Responsible Party: | New York State Psychiatric Institute |
ClinicalTrials.gov Identifier: | NCT01100255 |
Other Study ID Numbers: |
6906R/5883 |
First Posted: | April 8, 2010 Key Record Dates |
Results First Posted: | October 27, 2016 |
Last Update Posted: | February 20, 2017 |
Last Verified: | January 2017 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
OCD |
Compulsive Personality Disorder Obsessive-Compulsive Disorder Personality Disorders Mental Disorders Anxiety Disorders Ketamine 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 |