Status:

COMPLETED

Cortisol Suppression and Startle Responses in Posttraumatic Stress Disorder (PTSD)

Lead Sponsor:

Emory University

Collaborating Sponsors:

National Institute of Mental Health (NIMH)

Conditions:

Post Traumatic Stress Disorder

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

Posttraumatic stress disorder (PTSD) occurs in some people after exposure to events that cause extreme fear or helplessness. The incidence of war zones worldwide and the prevalence of violence in larg...

Detailed Description

The proposed study will provide innovative tools to tease apart the relationship between amygdala-dependent neurophysiology and HPA-axis sensitivity in a human clinical population. Investigators have ...

Eligibility Criteria

Inclusion

  • Able to give informed consent
  • Willing to participate in initial assessment and 2 full days of interviews and imaging visit
  • Able to understand English and no obvious deficit in comprehension or following directions
  • 18-65 years old

Exclusion

  • Mental Retardation (per clinical judgment of study physician)
  • Psychotic Disorder (per clinical judgment of study physician)
  • Acute suicidal ideation
  • Pregnancy
  • Positive urine drug screen
  • Active medical disorders contributing to psychiatric sx e.g. hypo or hyperthyroidism, SLE, advanced cirrhosis, etc. (per clinical judgment of study physician)

Key Trial Info

Start Date :

November 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2015

Estimated Enrollment :

165 Patients enrolled

Trial Details

Trial ID

NCT01477762

Start Date

November 1 2011

End Date

July 1 2015

Last Update

April 18 2017

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Grady Health System

Atlanta, Georgia, United States, 30303

Cortisol Suppression and Startle Responses in Posttraumatic Stress Disorder (PTSD) | DecenTrialz