Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Rush University Medical Center
With
National Institute of Mental Health (NIMH)
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female outpatients age 18-65 with a primary diagnosis of PTSD and associated sleep disturbance
Good physical health
Willingness and ability to comply with the requirements of the study protocol
You may not be if
Women pregnant, lactating, or of childbearing potential not using medically accepted contraception
Concurrent use of other psychotropic medications at least two weeks prior to baseline
Concurrent use of other anti-inflammatory medications or anti-cytokine medications. If used on an as-needed (PRN) basis, subjects may enter the study, but will be excluded from cytokine analyses
Concurrent use of beta-blockers less than one month prior to baseline
Serious medical illness or instability for which hospitalization may be likely within the next year
Seizure disorders with the exception of a history of febrile seizures if they occurred during childhood
Sleep apnea or restless leg syndrome
Concurrent psychotherapy initiated within 3 months of randomization or ongoing psychotherapy of any duration directed specifically toward treatment of PTSD and/or sleep disturbance
Patients with significant suicidal ideation
Current legal actions related to trauma or an ongoing relationship with assailant
Clareo Health | Eszopiclone for the Treatment of Posttraumatic Stress Disorder
