Post-Traumatic Stress Disorder (PTSD) and Seroquel

Completed · Not applicable

Conditions studied: Post-Traumatic Stress Disorder

In brief

This 8 weeks study will investigate therapeutic responses to Seroquel pharmacotherapy in PTSD.

Key facts

Study ID

NCT01066156

Run by

Cambridge Health Alliance

People needed

34

Starts

2010-02-01

Expected to finish

2015-03-01

Last updated by the study team

2017-05-30

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provision of written informed consent
• Fluency in English
• A diagnosis of PTSD
• No pregnancy
• Right-handedness

You may not qualify if…

• Pregnancy or lactation
• Any cognitive impairment that precludes informed consent
• Known intolerance or lack of response to Seroquel
• Previous enrollment or randomization of treatment in the present study
• Participation in another drug trial within 4 weeks prior enrollment into this study
• Patients with Diabetes Mellitus
• History of allergic reaction or hypersensitivity to Seroquel
• Contraindications to magnetic resonance imaging
• Treatment with an effective medication for PTSD

Where it is running

• Central Street Health Center — Somerville, Massachusetts, United States

Full record on ClinicalTrials.gov

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