Study of Combination Therapy for the Treatment of Adults with Post-Traumatic Stress Disorder

  • STATUS
    Recruiting
  • End date
    Jan 31, 2022
Updated on 21 April 2021

Summary

If you’ve experienced or witnessed a traumatic event and now have unwanted memories of the event, struggle with fear and anxiety, feel isolated from family and friends, or avoid situations that remind you of the trauma, you may have post-traumatic stress disorder (PTSD).

Description

This study will evaluate an investigational drug (which is approved in the U.S. for other uses) as combination treatment with an antidepressant that is approved in the United States for the treatment of PTSD. The results of this study will provide more information about the potential benefits of this treatment regimen for PTSD. Participation lasts about 17 weeks. You will have about 11 visits to the study site so the study doctors and staff can evaluate your health and progress through evaluation, laboratory tests, questionnaires and assessments and other procedures. These are conducted at no cost to you. A travel service can be arranged to bring you to the study site and back home again after your study visits.

Details
Condition Post-Traumatic Stress Disorders
Clinical Study IdentifierTX271616
Last Modified on21 April 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

You must be 18 to 65 years of age
You must be experiencing PTSD symptoms for at least 6 months prior to the study
Other criteria do apply

Exclusion Criteria

Females who are pregnant or breastfeeding cannot participate in this study
Have an unstable medical condition that could put you at undue risk
Other criteria do apply
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How to participate?

Step 1 Connect with a study center
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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