Yale School of Medicine

Research Studies at Yale

Research Studies at Yale

Facilitation of NMDA Receptor Function in Patients With Schizophrenia and co-Morbid Alcoholism

For Patients For Researchers

Conditions: Alcoholism; Schizophrenia

What is the purpose of this trial?

This placebo-controlled study is designed to evaluate the efficacy of glycine, an agonist of the glycine-B co-agonist site of the NMDA receptor, on alcohol consumption and craving as well as negative symptoms in schizophrenia.

Glycine will decrease the rewarding action of ethanol and reduce ethanol consumption. Also, glycine will improve negative symptoms and cognitive deficits in schizophrenia.


Dates: June 2003 -
Study Status: Recruiting

Who can participate?

Ages Eligible: 21 Years - 60 Years
Gender Eligible: Both

Inclusion Criteria:

  • DSM-IV diagnosis of schizophrenia or schizoaffective disorder
  • DSM-IV diagnosis of alcohol dependence
  • Stable treatment with typical or atypical antipsychotics

Exclusion Criteria:

  • Axis I diagnosis other than alcohol dependence, schizophrenia, schizoaffective disorder, OCD, and PTSD.
  • current drug dependence
  • evidence of significant hepatocellular injury evidence by abnormal SGOT or SGPT levels
  • history of seizures
  • diabetes and medical conditions that would alter glycine metabolism
  • positive pregnancy test
  • treatment with clozapine, naltrexone or disulfiram

Sponsors: Stanley Medical Research Institute, Yale University
Phase: Phase 2

First Received: June 15, 2006 
Last Updated: Jan 20, 2009
Clinicaltrials.gov ID: NCT00338598
Study HIC # 0209020915

Conditions: Alcoholism; Schizophrenia

Intervention: Drug: Glycine

What is the purpose of this trial?

This placebo-controlled study is designed to evaluate the efficacy of glycine, an agonist of the glycine-B co-agonist site of the NMDA receptor, on alcohol consumption and craving as well as negative symptoms in schizophrenia.

Glycine will decrease the rewarding action of ethanol and reduce ethanol consumption. Also, glycine will improve negative symptoms and cognitive deficits in schizophrenia.


show additional information...

Dates: June 2003 -
Study Status: Recruiting

Who can participate?

Ages Eligible: 21 Years - 60 Years
Gender Eligible: Both

Inclusion Criteria:

- DSM-IV diagnosis of schizophrenia or schizoaffective disorder

- DSM-IV diagnosis of alcohol dependence

- Stable treatment with typical or atypical antipsychotics

Exclusion Criteria:

- Axis I diagnosis other than alcohol dependence, schizophrenia, schizoaffective
disorder, OCD, and PTSD.

- current drug dependence

- evidence of significant hepatocellular injury evidence by abnormal SGOT or SGPT
levels

- history of seizures

- diabetes and medical conditions that would alter glycine metabolism

- positive pregnancy test

- treatment with clozapine, naltrexone or disulfiram


Additional Location

Connecticut

Sponsors: Stanley Medical Research Institute, Yale University
Phase: Phase 2

First Received: June 15, 2006 
Last Updated: Jan 20, 2009
Clinicaltrials.gov ID: NCT00338598
Study HIC # 0209020915

Participate in this trial

For more information about this trial, contact:

Elizabeth Ralevski, Ph.D.
203-932-5711 Ext. 4282
elizabeth.ralevski@yale.edu

Ismene Petrakis, M.D.
2-3-932-5711 Ext. 2244
ismene.petrakis@yale.edu


Yale Researcher

Petrakis, Ismene Leonida
Principal Investigator  

HIC # 0805003779