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The Effect of Imipramine on Early Information Processing
This study is ongoing, but not recruiting participants.
Sponsors and Collaborators: Bispebjerg Hospital
University of Copenhagen
Glostrup University Hospital,Copenhagen
The Danish Medical Research Council
The Lundbeck Foundation
Information provided by: Bispebjerg Hospital
ClinicalTrials.gov Identifier: NCT00206999
  Purpose

We wanted to compare the relation of two different psychophysiological paradigms (PrePulse Inhibition of the startle response = PPI and P50 suppression) to each other. Additionally, we wanted to test the effect of the combined serotonin- and noradrenaline re-uptake inhibitor, imipramine, on these measures. The primary hypothesis was that PPI and P50 gating would not correlate with each other at baseline. The secondary hypothesis was that increased noradrenergic and serotonergic activity would disrupt PPI as well as P50 gating.


Condition Intervention
Healthy Volunters
Drug: imipramine

Drug Information available for: Imipramine Imipramine hydrochloride
U.S. FDA Resources
Study Type: Interventional
Study Design: Diagnostic, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Pharmacodynamics Study
Official Title: Early Information Processing in Healthy Controls: Studies on the Relation Between Two Different Paradigms (PPI and P50ERP) and Effects of Pharmacological Interventions

Further study details as provided by Bispebjerg Hospital:

Primary Outcome Measures:
  • PrePulse Inhibition of the startle response
  • P50 ERP gating

Estimated Enrollment: 20
Study Start Date: September 2004
  Eligibility

Ages Eligible for Study:   18 Years to 35 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

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:

  • 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.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00206999

Locations
Denmark
Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychiatric Center Glostrup
Glostrup, Denmark, DK-2600
Sponsors and Collaborators
Bispebjerg Hospital
University of Copenhagen
Glostrup University Hospital,Copenhagen
The Danish Medical Research Council
The Lundbeck Foundation
Investigators
Study Director: Birte Glenthoj, MD, DMSc. Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Psychaitric Center Glostrup, Ndr. Ringvej, DK-2600 Glostrup, Denmark
  More Information

Center for Neuropsychiatric Schizophrenia Research (CNSR)  This link exits the ClinicalTrials.gov site

Study ID Numbers: 363052-2, KF 01-305/99, KF 11-061/03, KF 11-068/03, KF 11-096/04
Study First Received: September 11, 2005
Last Updated: September 11, 2006
ClinicalTrials.gov Identifier: NCT00206999  
Health Authority: Denmark: National Board of Health

Keywords provided by Bispebjerg Hospital:
Psychophysiology
PPI
P50 suppression
Imipramine

Study placed in the following topic categories:
Imipramine
Healthy

Additional relevant MeSH terms:
Neurotransmitter Uptake Inhibitors
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Adrenergic Agents
Adrenergic Uptake Inhibitors
Therapeutic Uses
Physiological Effects of Drugs
Psychotropic Drugs
Central Nervous System Agents
Pharmacologic Actions
Antidepressive Agents
Antidepressive Agents, Tricyclic

ClinicalTrials.gov processed this record on January 16, 2009