An interventional study of clonidine and clonidine in Schizophrenia, sponsored by Birte Glenthoj. Completed at 1 site in Denmark. Open to male participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-12-20.
Sponsored by Birte Glenthoj · Not applicable, Interventional, and Treatment
The investigators 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 either four doses (0.25 ug, 50 ug, 75 ug or 150 ug)of clonidine or placebo will be added to the current medical treatment of 20 male patients with schizophrenia on five occasions, separated by at least a week, after which they are tested in the Copenhagen Psychophysiological Test Battery (CPTB).In order to test the effects of clonidine in healthy volunteers, 20 healthy males will receive a fixed dose of 0.15 mg clonidine or placebo on two separate occasions separated by at least a week, after which they will be tested in the CPTB as well.
3,471 studies on the registry are indexed under Schizophrenia; 472 are open to participants now.
This study's planned enrollment of 40 is below the median of 70 across 2,872 interventional studies indexed under Schizophrenia.
Browse Schizophrenia studies →Birte Glenthoj is the lead sponsor of 7 studies on the registry; none are open to participants now.
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Exclusion Criteria:
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Controls:
Drug: clonidine
Drug: clonidine
Either placebo or 25 ug, 50 uG 75 ug or 150 ug of clonidine will be added to the current medication of patients with schizophrenia, who are stable on their current medication
Also known as: Catapressan
0.15 mg of clonidine will be administered to 20 healthy male volunteers
Also known as: Catapressan
The following psychophysiological measures:
Time frame: prospective
Prepulse Inhibition og the Startle Response (PPI)
Time frame: Once, 3.5 hrs after intake of capsule
P50 suppression
Time frame: Once, 3.5 hrs after intake of capsule
P300 Event Related Potential
Time frame: Once, 3.5 hrs after intake of capsule
Mismatch negativity
Time frame: Once, 3.5 hrs after intake of capsule
PANSS
Time frame: 5 times hourly after intake of capsule
This study is completed, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.
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Birte Glenthoj