Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:01 AM
Ignite Modification Date:
2025-12-25 @ 2:01 AM
NCT ID:
NCT01664260
Eligibility Criteria:
Inclusion Criteria:
* 20-65 year-old male or female
* Posttraumatic stress disorder diagnosed by SCID-IV
* Written informed consent
Exclusion Criteria:
* Medication treatment for posttraumatic stress disorder within 2 weeks
* Neurologic disease (eg., penetrating or open head injury, epilepsy, multiple sclerosis, brain tumor, cerebrovascular diseases)
* Any other axis I psychiatric disorder
* IQ below 80
* Contraindications to magnetic resosnance imaging (e.g., pacemaker implantation, claustrophobia, etc.)
* Any psychotropic medication within 2 weeks
* Unstable medical illness or severe abnormality in laboratory test at screening assessment
* Women who are pregnant, breastfeeding, or planning pregnancy
* History of myocardial infarction within 6 months
* Current diagnosis of duodenal ulcer or asthma
* Contraindications to drugs used in the study (e.g., epilepsy, uncontrolled narrow-angle glaucoma, etc.)
* Allergy or intolerance to the study drug
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
65 Years
Study:
NCT01664260
Study Brief:
Protocol Section:
NCT01664260