D-Cycloserine Augmentation of Exposure and Response Prevention Treatment for Obsessive-Compulsive Disorder

This study has been withdrawn prior to enrollment.
(PI left the university)
Sponsor:
Collaborator:
Obsessive Compulsive Foundation
Information provided by (Responsible Party):
University of Florida
ClinicalTrials.gov Identifier:
NCT00257361
First received: November 18, 2005
Last updated: September 16, 2011
Last verified: August 2011

November 18, 2005
September 16, 2011
July 2005
 
YBOCS
Same as current
Complete list of historical versions of study NCT00257361 on ClinicalTrials.gov Archive Site
Response rate
Same as current
 
 
 
D-Cycloserine Augmentation of Exposure and Response Prevention Treatment for Obsessive-Compulsive Disorder
D-Cycloserine Augmentation of Exposure and Response Prevention Treatment for Obsessive-Compulsive Disorder

We propose to undertake an initial study of DCS to determine whether it has any short-term clinical benefits when added to standard ERP therapy in adults with OCD.

Exposure and response prevention (ERP) has proven efficacy for OCD treatment in adults. Yet, ERP does not help all individuals, and those who benefit often remain somewhat symptomatic. Behavioral models for OCD treatment are based on two components. First, fears are acquired by the development of an association between a neutral stimulus and an aversive stimulus such the former acquires the aversive properties of the latter. The neutral stimulus is then designated as a conditioned stimulus (CS), and the original aversive stimulus is called an unconditioned stimulus (UCS). Second, the acquired fears can be unlearned through presentation of the CS in the absence of the UCS, a process known as extinction. On a neural level, ERP incorporates similar mechanisms to those involved in fear conditioning. Antagonists at the glutamatergic NMDA receptor, which is involved in learning and memory, block both fear learning and extinction. D-Cycloserine (DCS), a partial agonist at the N-methyl-D-aspartate (NMDA) glutamate receptor subtype, augments learning in animals and humans. Clinical application in animals and humans suggest that DCS facilitates the fear extinction process when taken prior to exposure to feared stimuli. An initial trial in acrophobic adults provided support for acute DCS dosing as facilitating extinction to fear. Given that ERP is based on extinction, it follows that DCS may augment ERP therapy providing enhanced treatment effects. With this in mind, we propose to undertake an initial study of DCS to determine whether it has any short-term clinical benefits when added to standard ERP therapy in adults with OCD.

Interventional
Phase 2
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Double-Blind
Obsessive Compulsive Disorder
Drug: D-Cycloserine
 
 

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
40
 
 

Inclusion Criteria:

  1. a principal diagnosis of OCD assigned at pre-treatment, derived from the ADIS-IV, with a clinical severity rating of 4 or above;
  2. 18-65 years of age; and,
  3. an IQ of ³ 80.

Exclusion Criteria:

  1. positive diagnosis of schizophrenia, other psychotic disorder, pervasive developmental disorder, organic brain syndrome, or mental retardation;
  2. do not speak English;
  3. are unwilling to attend twice weekly sessions; or,
  4. is pregnant, breast feeding a child, or attempting to become pregnant (see below rationale)
Both
18 Years to 65 Years
 
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00257361
IRB Protocol #639-2004, 00053428
No
University of Florida
University of Florida
Obsessive Compulsive Foundation
Principal Investigator: Eric Storch, Ph.D. University of Florida
University of Florida
August 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP