PTSD Research Study – Post Traumatic Stress Disorder

Updated on 23 November 2020


Summit Research Network is enrolling volunteers in a new clinical trial for post-traumatic stress disorder (PTSD) in adults. This trial will evaluate the safety and effectiveness of a combination of two medications in the treatment of PTSD.

Study participation will last from 16-18 weeks and includes approximately 11 visits to the research center. After a screening period of up to 2 weeks, qualified participants will be randomly assigned to one of the study treatment groups.



Study Participants Receive:

  • Study-related physical exams, laboratory tests, and ECG
  • Study medication for PTSD
  • Ongoing research related study visits and monitoring with our experienced medical and clinical staff As with all studies at Summit Research Network, if you qualify for this research study and choose to participate, all research related care, evaluations, study medication, and office visits will be provided at no cost. Insurance is not required for study related visits, procedures or evaluations. Compensation up to $825.00 may be available for qualified participants completing a study. To learn more and see if you may qualify, call Summit Research Network at (503) 228-2273 or visit us at
  • Details
    Clinical Study IdentifierTX239670
    Last Modified on23 November 2020


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    Inclusion Criteria

    Is your age between 18 yrs and 65 yrs?
    Gender: Male or Female
    Males and females age 18 to 65
    Participants either have a diagnosis of PTSD or are experiencing symptoms they believe are related to PTSD
    Participants must be generally healthy. Any other current medical conditions are stable and well controlled
    Other criteria may apply
    If you are unsure of your diagnosis, or whether or not another condition or medication may be allowed in this trial, please contact the study team. We may be able to help identify whether or not you may qualify for the study
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    How to participate?

    Step 1 Connect with a site
    What happens next?
    • You can expect the study team to contact you via email or phone in the next few days.
    • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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    Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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    If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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    Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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