Prevention/Reduction of ASRs and PTSD to Sustain Civilian Performance With Sublingual Cyclobenzaprine HCl (TNX-102 SL)

Abroad (travel likely)RecruitingPHASE2

Conditions

Acute Stress Reaction · Acute Stress Disorder · Neurocognitive Function · Post-traumatic Stress

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations
  • University of Alabama at Birmingham, Birmingham, Alabama, United States

    Contact: Study coordinator (Whitney Taylor)
    Contact: Principal Investigator (Lauren Walter)
  • Indiana University, Indianapolis, Indiana, United States

    Contact: Study coordinator (Leah Emmons) · ldemmons@iu.edu · 463-274-2373
    Contact: Principal Investigator (Paul Musey, MD)
  • University of Kansas Medical Center, Kansas City, Kansas, United States

    Contact: Study coordinator (Lucas Lemar) · llemar@kumc.edu · 913-588-3580
    Contact: Principal Investigator (Lindsay Maguire, MD)
    Chad Cannon, MD (Sub-investigator)
  • Washington University in St. Louis, St Louis, Missouri, United States

    Contact: Study coordinator (Jamie Mills) · jamiem@wustl.edu · 314-273-1382
    Contact: Principal Investigator (Stacey House, MD)
  • Cooper University Health System, Camden, New Jersey, United States

    Contact: Study coordinator (Dylan Kurowsky)
    Contact: Principal Investigator (Christopher Jones)
  • The Ohio State University, Columbus, Ohio, United States

    Contact: Study coordinator (Hawa Sall)
    Contact: Principal Investigator (Michael Lyons)
  • Rhode Island Hospital, Providence, Rhode Island, United States

    Contact: Study coordinator (Carolyn Ortega) · cortega@lifespan.org · 401-444-6619
    Contact: Study coordinator (Sarah Tokarz) · stokarz1@lifespan.org · 401-606-9815
    Contact: Principal Investigator (Adam Aluisio, MD)
  • The Miriam Hospital, Providence, Rhode Island, United States

    Contact: Study coordinator (Carolyn Ortega) · cortega@lifespan.org · 401-444-6619
    Contact: Principal Investigator (Adam Aluisio, MD)
  • University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States

    Contact: Study coordinator (Stephanie Perez)
    Contact: Principal Investigator (Ralph Riviello)
Study leads
  • Samuel McLean, MD

    Principal Investigator

    University of North Carollina at Chapel Hill

  • Christopher Jones, MD

    Principal Investigator

    Cooper University Health Care