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CompletedNCT00206934Updated Sep 19, 2011

The Effects of Increased Central Serotonergic Activity on Information Processing

An interventional study of Escitalopram and escitaolpram in Healthy Volunteers, sponsored by University of Copenhagen. Completed at 1 site in Denmark. Open to male participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-09-19.

Sponsored by University of Copenhagen · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Male
01

Study summary

It is of great clinical relevance to know if selective serotonin re-uptake inhibitors affect information processing. Our hypothesis was that aspects of information processing would be disturbed whereas others would improve.

Read the detailed description

Numerous studies point to an increased serotoninergic activity in schizophrenia. Additionally, patients with schizophrenia often show reduced filtering of sensory information, which is reflected in reduced P50 suppression and reduced prepulse inhibition of the startle refex (PPI). Currently, the reports in literature on the effects of serotonergic agonists on sensory gating in humans are inconclusive. In an initial study performed in our laboratory, however, we found reduced P50 suppression following administration of imipramine (a combined serotonin- and noradrenalin reuptake inhibitor) to healthy volunteers. This result provides evidence for the involvement of either serotonergic, noradrenergic, or a combination of both pathways in sensory gating. In numerous animal studies however, sensory gating is reduced by agonists of 5-HT, which suggests a serotonergic, rather than a noradrenergic, involvement in sensory gating. Therefore, in a follow-up study, the effects of a selective serotonin reuptake inhibitor (escitalopram) will be investigated on sensory gating parameters of healthy volunteers. To further extend the data of our initial study, the subjects will additionally be tested for two more 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 be a double blind, placebo controlled experiment, in which a single dose of escitalopram or placebo will be given to healthy, non-smoking male volunteers on two occasions, separated by at least a week, after which the subjects will be tested in the psychophysiological test battery.

02

Conditions studied

  • Healthy Volunteers

Keywords

  • PPI
  • P50 suppression
  • P300
  • mismatch negativity
  • escitalopram
03

In context

Lead sponsor

University of Copenhagen is the lead sponsor of 450 studies on the registry; 61 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • 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. Positive urine screening for amphetamine, cocaine, cannabis, or esctacy.
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Single group
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
40 participants (actual)

Study arms

  • Placebo comparator
    1

    Drug: Escitalopram

  • Placebo comparator
    2

    Drug: escitaolpram

Interventions

  • DrugEscitalopram

    Either 10 mg of escitalopram or placebo will be administered to a group of healthy volunteers

    Also known as: Cipralex

  • Drugescitaolpram

    Either 15 mg of escitalopram or placebo will be administered to healthy volunteers

    Also known as: Cipralex

06

What researchers measure

Primary outcomes

  1. The PPI (Prepulse Inhibition of the Startle Response) task

    Time frame: Once, 3.5 hrs after intake of capsule

  2. The P50 Suppression task

    Time frame: Once, 3.5 hrs after intake of capsule

  3. The P300 ERP task

    Time frame: Once, 3.5 hrs after intake of capsule

  4. The mismatch negativity (MMN) task

    Time frame: Once, 3.5 hrs after intake of capsule

07

Study locations

1 site
  • Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychiatric Center Glostrup
    Glostrup, DK-2600, 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 Sep 19, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00206934
Lead sponsor
University of Copenhagen
Collaborators
Lundbeck Foundation, Glostrup University Hospital, Copenhagen
First posted
Sep 21, 2005
Start date
Mar 2005
Primary completion
Mar 2006
Completion
Mar 2006
Last update
Sep 19, 2011

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 ↗

Not currently enrolling

This study is completed, as verified in Jul 2008. You cannot join it, but the record below documents what was studied.

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