Status:

COMPLETED

Effect of D-cycloserine on Extinction of Fear Conditioning

Lead Sponsor:

National Institute of Mental Health (NIMH)

Conditions:

Fear

Eligibility:

All Genders

18-50 years

Brief Summary

This study will evaluate whether the drug D-cycloserine (DCS) can improve a type of learning called classical conditioning, in which the brain learns to associate neutral stimuli with stimuli that eli...

Detailed Description

This protocol examines the effect of two drugs on fear conditioning. Study 1 tests assess whether D-cycloserine (DCS) facilitates extinction of fear conditioning and acquisition of eyeblink conditioni...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Subjects must meet the following inclusion criteria in order to participate in the study:
  • Male or female volunteers ages 18-50 years old.
  • Judged to be in good physical health on the basis of medical history and physical examination.
  • Able to understand procedures and agree to participate in the study by giving written informed consent.
  • EXCLUSION CRITERIA:
  • Exclusion criteria will be different for studies with and without (pilot study) DCS. Subjects will be excluded from the DCS study if they meet the following exclusion criteria:
  • History of allergy to D-cycloserine (study 1) or nimodipine (study 2).
  • No clinically significant organ disease by history, physical examination, LFT's, TFT's, electrolytes, BUN, creatinine, Ca+2, Mg+2, urinalysis, CBC with differential, and EKG.
  • History of any disease, which in the investigators' opinion may confound the results of the study, including, but not limited to, history of organic mental disorders, seizure, or mental retardation.
  • Any significant medical or neurological problems (e.g. cardiovascular illness, respiratory illness, neurologic illness, seizure, stroke, multiple sclerosis, Alzeimer's disease, etc.)
  • Past or current substance dependence.
  • Presence of psychotropic medications or illicit substance in urine.
  • Positive pregnancy test.
  • Current or past Axis I psychiatric disorders as identified with the Structured Clinical Interview for DSM-IV-TR axis disorders, non-patient edition (SCID-np).
  • Current psychotropic medication.
  • Impaired hearing defined as inability to hear a 40 dB(HL) pure tone in the 1000- to 4000 Hz span. Reduced or excessive startle reactivity.
  • Neurological symptoms that affect the arms or wrist (e.g., carpal tunnel syndrome).

Exclusion

    Key Trial Info

    Start Date :

    April 3 2002

    Trial Type :

    OBSERVATIONAL

    End Date :

    February 1 2008

    Estimated Enrollment :

    160 Patients enrolled

    Trial Details

    Trial ID

    NCT00352586

    Start Date

    April 3 2002

    End Date

    February 1 2008

    Last Update

    July 2 2017

    Active Locations (1)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (1 locations)

    1

    National Institutes of Health Clinical Center, 9000 Rockville Pike

    Bethesda, Maryland, United States, 20892