We have research studies available for adults with Post-Traumatic Stress Disorder (PTSD). The purpose of these research studies is to find better and safer medications for individuals with PTSD.
The investigational medication will be provided at no cost and compensation is provided for time and travel. No health insurance is required to participate in any of our PTSD studies.
Post-Traumatic Stress Disorder
What is Post-Traumatic
Stress Disorder (PTSD)?
Post-Traumatic Stress Disorder is a severe condition that can occur in people who have experienced or witnessed a traumatic event such as a natural disaster, a serious accident, a terrorist act, war/combat, rape or other violent personal assault.
PTSD does not just happen to combat veterans. It can occur in all people of any ethnicity, nationality or culture, and age.
People with PTSD have intense, disturbing thoughts and feelings related to their experience that last long after the traumatic event has ended. They may relive the event through flashbacks or nightmares; they may feel sadness, fear or anger; and they may feel detached or estranged from other people. People with PTSD may avoid situations or people that remind them of the traumatic event.1
Do i qualify?
If you answer YES to all of the following questions then you may qualify for our PTSD clinical trials.
1. Are you over the age of 18?
2. Do you currently have PTSD symptoms?
3. Are you willing to take study medication?
Final eligibility is determined during a screening visit at our study site at Orange. During this visit, you will:
Meet with a professional physician, psychiatrist, or psychologists and be interviewed about your mental and physical health
Review additional information
Undergo a physical examination and have your vitals taken
If you qualify and decide to participate:
A study doctor will closely monitor you, your symptoms, and overall health
All study-related medical care and study medication will be provided at no cost
Transportation may be provided at no cost if you need assistance
You will sign an Informed Consent Form (ICF) which outlines which procedures you can expect during each visit
You will be compensated for each completed visit
*A list of common procedures involved when participating in a clinical trial can be found here.