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 @ 12:44 AM
Ignite Modification Date:
2025-12-25 @ 12:44 AM
NCT ID:
NCT00691067
Eligibility Criteria:
Inclusion Criteria:
* Veteran of the 1991 Gulf War
* Veteran meets criteria for multisymptom illness
Exclusion Criteria:
* Veteran lacks the capacity to provide consent.
* Veteran has a major medical or neurological disorder or traumatic brain injury
* Veteran has morning plasma cortisol level less than 5 mcg/dl or a history of adrenal insufficiency
* Veteran is taking oral corticosteroids
* Veteran has a lifetime diagnosis of schizophrenia, schizoaffective disorder or bipolar disorder
* Veteran has been psychiatrically hospitalized or attempted suicide within the previous 2 years
* Veteran has current suicidal ideation
* Veteran is pregnant or breastfeeding or plans to become pregnant within the year (male or female) not willing to use appropriate forms of contraception during the study and for at least 90 days post treatment.
* Women veterans with diseases of the uterus by history or a family history of uterine cancer
* Known allergy to mifepristone
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
35 Years
Study:
NCT00691067
Study Brief:
Protocol Section:
NCT00691067