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Completed

NCT Number: NCT00222235

Adjunctive Treatment for Decreasing Symptoms of Schizophrenia

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.

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Key information

Age range

18 year–54 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Ezrath Nashim Association, Sarah Herzog Memorial Hospital, Jerusalem, Israel

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

D-cycloserine

Drug

Glycine

Drug

Placebo

Drug

Primary outcomes

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

  2. change from baseline on neurocognitive battery measured at 16 weeks.

Secondary outcomes

  1. change in psychotic and depressive symptoms measured at 4,8,12, and 16 weeks.

  2. changes in extrapyramidal side effects at 4,8,12 and 16 weeks.

Sponsors and collaborators

Lead sponsor

University of Maryland, Baltimore

Other

Collaborators

  • Nathan Kline Institute for Psychiatric Research
  • National Institute of Mental Health (NIMH)
  • Sarah Herzog Hospital
  • The Zucker Hillside Hospital
  • University of California, Los Angeles
  • University of Maryland, College Park

Registry information

Official study title

Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST)

Important dates

Study start
2000
Primary completion
2004
Study completion
2004
First posted
Sep 22, 2005
Registry last updated
Aug 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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