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CompletedNCT00206986Updated Dec 20, 2013

Will Decreased Noradrenergic Activity Normalize Information Processing in Patients With Schizophrenia?

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

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Male
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Study summary

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.

Read the detailed description

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.

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Conditions studied

  • Schizophrenia

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Keywords

  • Schizophrenia
  • Information processing
  • PPI
  • P50 gating
  • P300
  • mismatch negativity
  • clonidine
03

In context

Schizophrenia

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 →

Lead sponsor

Birte Glenthoj is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    1

    Drug: clonidine

  • Experimental
    2

    Drug: clonidine

Interventions

  • Drugclonidine

    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

  • Drugclonidine

    0.15 mg of clonidine will be administered to 20 healthy male volunteers

    Also known as: Catapressan

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What researchers measure

Primary outcomes

  1. The following psychophysiological measures:

    Time frame: prospective

  2. Prepulse Inhibition og the Startle Response (PPI)

    Time frame: Once, 3.5 hrs after intake of capsule

  3. P50 suppression

    Time frame: Once, 3.5 hrs after intake of capsule

  4. P300 Event Related Potential

    Time frame: Once, 3.5 hrs after intake of capsule

  5. Mismatch negativity

    Time frame: Once, 3.5 hrs after intake of capsule

  6. PANSS

    Time frame: 5 times hourly after intake of capsule

07

Study locations

1 site
  • Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychiatric Center Glostrup
    Copenhagen NV, DK-2400, Denmark
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 20, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00206986
Lead sponsor
Birte Glenthoj
Collaborators
University of Copenhagen, Lundbeck Foundation, Glostrup University Hospital, Copenhagen
Responsible party
Birte Glenthoj (Professor, University of Copenhagen) — Sponsor-investigator
First posted
Sep 21, 2005
Start date
May 2005
Primary completion
Dec 2011
Completion
Dec 2011
Last update
Dec 20, 2013

Study contacts

Birte Glenthoj, MD, DMSc.
study director · Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychaitric Center Glostrup, Ndr. Ringvej, DK-2600 Glostrup, Denmark

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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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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