Schizophrenia Sensory Gating Deficit With Quetiapine
2 other identifiers
observational
20
1 country
1
Brief Summary
The purpose of this study is the use of magnetoencephalography or MEG (a machine that measures magnetic activity in your brain) and electroencephalography or EEG (a technique that measures electrical activity in your brain) to study how sounds are processed in individuals with schizophrenia after three months of taking the antipsychotic medication quetiapine.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2004
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2004
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2006
CompletedFirst Submitted
Initial submission to the registry
September 27, 2007
CompletedFirst Posted
Study publicly available on registry
September 28, 2007
CompletedDecember 31, 2007
September 1, 2007
September 27, 2007
December 20, 2007
Conditions
Keywords
Interventions
Eligibility Criteria
You may qualify if:
- Patient Population
- Diagnosis of Schizophrenia as determine by the Structured Clinical Interview for DSM-IV
- No comorbid diagnosis of PTSD
- responders to quetiapine, determined by continuous treatment at the same dose of quetiapine and absence of psychiatric hospitalization for at least 3 months
- No history of drug dependency in their lifetime
- No history of alcohol or other substance abuse in the 6 months prior to entry into the study
- No history of head injury with loss of consciousness for more than 5 minutes
- No history of seizure disorder
- No mood stabilizing agents
- Between 18-65 and
- Able to sign informed consent
- Normal Controls
- Matched in age and gender to patient population
- No history of psychiatric dysfunction or alcohol or other substance dependence in their lifetime as determine by the SCID
- No history of alcohol or other substance abuse in the previous 6 months
- +5 more criteria
You may not qualify if:
- Subjects will be excluded from participating in this study if they:
- Require treatment with a mood stabilizer
- Have had an inpatient hospitalization in the past 3 months
- Have a history of a neurological disorder
- Have any other axis I diagnosis besides schizophrenia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- New Mexico VA Healthcare Systemlead
- AstraZenecacollaborator
Study Sites (1)
New Mexico VA Healthcare System
Albuquerque, New Mexico, 87108, United States
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jose M Canive, MD
New Mexico VA Heathcare System / BRINM
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- FED
Study Record Dates
First Submitted
September 27, 2007
First Posted
September 28, 2007
Study Start
April 1, 2004
Study Completion
March 1, 2006
Last Updated
December 31, 2007
Record last verified: 2007-09