Status:
TERMINATED
Enhanced Consent for Symptom Provocation Research
Lead Sponsor:
Georgetown University
Conditions:
Trauma
Eligibility:
FEMALE
18-55 years
Phase:
NA
Brief Summary
The overall goal of the proposed study is to insure the protection and safety of human subjects who have been previously exposed to interpersonal traumatic events and who are participants in symptom p...
Detailed Description
The overall goal of the proposed study is to insure the protection and safety of human subjects who have been previously exposed to interpersonal traumatic events and who are participants in symptom p...
Eligibility Criteria
Inclusion
- nonsmoker
- female
- between 18-55
- experienced trauma
- willing to have a brain scan
- provide consent
Exclusion
- alcohol abuse or dependence
- bipolar disorder
- suicidal intent
- metal in the body or anything else that would interfere with an MRI
- claustrophobia or inability to lie still for 45 minutes
- receiving current counseling
- on certain antidepressants, benzodiazepines, or other psychotropic medication
- pregnant or nursing
Key Trial Info
Start Date :
April 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2014
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT01809899
Start Date
April 1 2009
End Date
August 1 2014
Last Update
January 24 2018
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