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Clinical Trials/EUCTR2005-002701-23-AT
EUCTR2005-002701-23-ATActive, not recruitingNot Applicable

Escitalopram versus Citalopram Treatment effects on cortical and subcortical activity assessed by pharmacological fMRI

Siegfried Kasper, O.Univ.Prof.Dr.Dr.h.c.0 sites18 target enrollmentStarted: October 7, 2005Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
18

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Sex
All

Inclusion Criteria

  • Age 18 - 55 years.
  • Male or female healthy volunteers.
  • No history of drug or alcohol abuse.
  • Normal laboratory values.
  • Normotension (blood pressure less than 140/90).
  • No past or present history of psychiatric disorders or major medical illness.
  • Negative urine pregnancy test in women at the screening visit & prior to each fMRI
  • Signed informed consent form.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years)
  • F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • Clinically relevant abnormalities on a general physical examination and routine laboratory screening.
  • Ingestion of any medication that might interfere with the study medication within 4 week prior to screening visit.
  • Family history of diabetes or obesity

Investigators

Sponsor
Siegfried Kasper, O.Univ.Prof.Dr.Dr.h.c.

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