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Will Decreased Noradrenergic Activity Normalize Information Processing in Patients With Schizophrenia?
This study is ongoing, but not recruiting participants.
Study NCT00206986   Information provided by Bispebjerg Hospital
First Received: September 12, 2005   Last Updated: September 11, 2006   History of Changes

September 12, 2005
September 11, 2006
May 2005
 
  • The following psychophysiological measures:
  • Prepulse Inhibition og the Startle Response (PPI)
  • P50 suppression
  • P300 Event Related Potentials
  • Mismatch negativity
  • PANSS
Same as current
Complete list of historical versions of study NCT00206986 on ClinicalTrials.gov Archive Site
 
 
 
Will Decreased Noradrenergic Activity Normalize Information Processing in Patients With Schizophrenia?
Will Decreased Noradrenergic Activity Normalize Information Processing in Patients With Schizophrenia?

We want to try to improve information processing in schizophrenic patients via pharmacological intervention. The hypothesis is that decreased noradrenergic activity will normalize information processing (PPI, P50 gating, P300, and mismatch negativity) in patients with schizophrenia

A number of reports in literature provide evidence for, among others, an increased central noradrenergic activity in schizophrenia. In addition to this increased noradrenergic activity, patients with schizophrenia often show reduced filtering of sensory information, which is reflected in reduced P50 suppression and reduced prepulse inhibition of the startle reflex (PPI). In two separate initial studies in our laboratory, we found reduced sensory gating following administration of imipramine (a combined noradrenergic and serotonergic agonist) and desipramine (a highly specific noradrenergic agonist) to healthy volunteers. This provides evidence for a direct causal relation between the increased noradrenergic activity and the disturbed gating of sensory information, as both commonly found in patients with schizophrenia. Therefore, in a follow-up study, the effects of a noradrenergic antagonist will be investigated on the sensory gating of patients with schizophrenia. To further extend the data of our initial studies, the patients will additionally be tested for two psychophysiological parameters of attention that are usually found to be disturbed in patients with schizophrenia, i.e. mismatch negativity and selective attention. The design will conform to a double blind, placebo controlled experiment, in which a single dose of 0.2 mg of clonidine will be added to the current medical treatment of 20 male patients with schizophrenia on two occasions, separated by at least a week, after which they are tested in a psychophysiological test battery.

 
Interventional
Allocation:  Randomized
Control:  Placebo Control
Endpoint Classification:  Pharmacodynamics Study
Intervention Model:  Crossover Assignment
Masking:  Double-Blind
Primary Purpose:  Diagnostic
Schizophrenia
Drug: clonidine
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
40
February 2006
 

Inclusion Criteria:

  • Patients:

    • Male subjects
    • Meeting the DSM-IV diagnosis of schizophrenia
  • Controls:

    • Male subjects
    • Good Physical and Mental Health meeting criteria "never mentally ill", which will be evaluated with a medical history checklist
    • Non smokers

Exclusion Criteria:

  • Patients:

    • A P50 suppression or PPI score falling within a range of 10 percent above or below the mean score of the healthy control group
  • Controls:

    • Current use of any medication
    • Any subject who has received any investigational medication within 30 days prior to the start of this study
    • History of neurologic illness
    • History of psychiatric illness in first-degree relatives, evaluated with DSM-IV criteria
    • History of alcohol and drug abuse.
Male
18 Years to 35 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00206986
 
363037-2, KF 11-261729
Bispebjerg Hospital
  • University of Copenhagen
  • Lundbeck Foundation
  • Glostrup University Hospital, Copenhagen
Study Director: Birte Glenthoj, MD, DMSc. Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychaitric Center Glostrup, Ndr. Ringvej, DK-2600 Glostrup, Denmark
Bispebjerg Hospital
September 2006

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