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Adjunctive Treatment for Decreasing Symptoms of Schizophrenia

Primary Purpose

Schizophrenia, Schizoaffective Disorder

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
d-cycloserine
glycine
placebo
Sponsored by
University of Maryland, Baltimore
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, schizoaffective disorder, negative symptoms, cognitive impairments

Eligibility Criteria

18 Years - 54 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: diagnosis of schizophrenia or schizoaffective disorder stable, enduring negative symptoms above a certain level (SANS >19) clinically stable, with psychotic symptoms measured on BPRS below 19, anxiety/depression on BPRS below 15 extrapyramidal symptoms measured on SAS below 9 on stable antipsychotic regimen (not including clozapine) Exclusion Criteria: alcohol or substance dependence within last six months alcohol or substance abuse within last month organic brain disorder medical condition whose pathology or treatment could alter the presentation or treatment of schizophrenia, including active tuberculosis or tuberculosis treatment, kidney stones, and uncontrolled diabetes mellitus Female participants could not be pregnant and were required to be using a documented method of contraception.

Sites / Locations

  • UCLA/VA Greater Los Angeles Health Care System
  • Maryland Psychiatric Research Center
  • Zucker Hillside Hospital
  • Nathan S Kline Institute for Psychiatric Research
  • Ezrath Nashim Association, Sarah Herzog Memorial Hospital

Outcomes

Primary Outcome Measures

changes from baseline in negative symptoms measured on SANS at 4,8,12 and 16 weeks.
change from baseline on neurocognitive battery measured at 16 weeks.

Secondary Outcome Measures

change in psychotic and depressive symptoms measured at 4,8,12, and 16 weeks.
changes in extrapyramidal side effects at 4,8,12 and 16 weeks.

Full Information

First Posted
September 13, 2005
Last Updated
August 15, 2019
Sponsor
University of Maryland, Baltimore
Collaborators
National Institute of Mental Health (NIMH), The Zucker Hillside Hospital, Nathan Kline Institute for Psychiatric Research, University of California, Los Angeles, Sarah Herzog Hospital, University of Maryland, College Park
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1. Study Identification

Unique Protocol Identification Number
NCT00222235
Brief Title
Adjunctive Treatment for Decreasing Symptoms of Schizophrenia
Official Title
Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
January 2000 (Actual)
Primary Completion Date
June 2004 (Actual)
Study Completion Date
June 2004 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Maryland, Baltimore
Collaborators
National Institute of Mental Health (NIMH), The Zucker Hillside Hospital, Nathan Kline Institute for Psychiatric Research, University of California, Los Angeles, Sarah Herzog Hospital, University of Maryland, College Park

4. Oversight

5. Study Description

Brief Summary
This study will determine the effectiveness of treatment with glycine or d-cycloserine in addition to a normal antipsychotic regimen in improving negative symptoms and cognitive impairments in patients with schizophrenia.
Detailed Description
A double-blind, placebo controlled clinical trial to examine whether adjunctive treatment with glycine or d-cycloserine, compared to placebo, will improve negative symptoms and cognitive impairments in patients with schizophrenia who remain on their normal antipsychotic regimen. Multicenter, randomized, double-blinded placebo controlled parallel-groups clinical trial designed to test the hypothesis that interventions (glycine or d-cycloserine) intended to increase glutamatergic activity by action at the NMDA receptor will reduce persistant negative symptoms and cognitive impairments of patients with schizophrenia or schizoaffective disorder. After an initial screening phase to establish clinical stability and eligibility, patients were assigned to one of three adjunctive treatments (placebo, d-cycloserine or glycine)for 16 weeks of double-blind treatment. Patients remained on a stable dose of antipsychotic therapy (other than clozapine) throughout the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder
Keywords
schizophrenia, schizoaffective disorder, negative symptoms, cognitive impairments

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
240 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
d-cycloserine
Intervention Type
Drug
Intervention Name(s)
glycine
Intervention Type
Drug
Intervention Name(s)
placebo
Primary Outcome Measure Information:
Title
changes from baseline in negative symptoms measured on SANS at 4,8,12 and 16 weeks.
Title
change from baseline on neurocognitive battery measured at 16 weeks.
Secondary Outcome Measure Information:
Title
change in psychotic and depressive symptoms measured at 4,8,12, and 16 weeks.
Title
changes in extrapyramidal side effects at 4,8,12 and 16 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
54 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of schizophrenia or schizoaffective disorder stable, enduring negative symptoms above a certain level (SANS >19) clinically stable, with psychotic symptoms measured on BPRS below 19, anxiety/depression on BPRS below 15 extrapyramidal symptoms measured on SAS below 9 on stable antipsychotic regimen (not including clozapine) Exclusion Criteria: alcohol or substance dependence within last six months alcohol or substance abuse within last month organic brain disorder medical condition whose pathology or treatment could alter the presentation or treatment of schizophrenia, including active tuberculosis or tuberculosis treatment, kidney stones, and uncontrolled diabetes mellitus Female participants could not be pregnant and were required to be using a documented method of contraception.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William T Carpenter, MD
Organizational Affiliation
Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicien
Official's Role
Study Chair
Facility Information:
Facility Name
UCLA/VA Greater Los Angeles Health Care System
City
Los Angeles
State/Province
California
ZIP/Postal Code
90073
Country
United States
Facility Name
Maryland Psychiatric Research Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21228
Country
United States
Facility Name
Zucker Hillside Hospital
City
Glen Oaks
State/Province
New York
ZIP/Postal Code
11004
Country
United States
Facility Name
Nathan S Kline Institute for Psychiatric Research
City
Orangeburg
State/Province
New York
ZIP/Postal Code
10982
Country
United States
Facility Name
Ezrath Nashim Association, Sarah Herzog Memorial Hospital
City
Jerusalem
ZIP/Postal Code
91531
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
17898352
Citation
Buchanan RW, Javitt DC, Marder SR, Schooler NR, Gold JM, McMahon RP, Heresco-Levy U, Carpenter WT. The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST): the efficacy of glutamatergic agents for negative symptoms and cognitive impairments. Am J Psychiatry. 2007 Oct;164(10):1593-602. doi: 10.1176/appi.ajp.2007.06081358.
Results Reference
derived

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Adjunctive Treatment for Decreasing Symptoms of Schizophrenia

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