At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 18 enrolled
Drug / intervention
Riluzoledrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
An Investigation of the Effects of Riluzole in Patients With Post-Traumatic Stress Disorder (PTSD)
In Brief
A Phase 1 clinical trial evaluating Riluzole for PTSD. Completed, enrolled 18 participants across 1 site.
Detailed Summary
This open label study will evaluate the safety and efficacy of riluzole in patients with PTSD. Patients will receive riluzole 50mg twice per day orally for 12 weeks as outpatient, with a one month follow up at week 16.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPTSD
CountriesUnited States
CollaboratorsNational Center for PTSD
Timeline
Phase 1CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedDec 2013
Enrollment StartJan 2014
Primary CompletionJan 2020
TodayJul 2026
First PostedDec 24, 2013
Enrollment StartJan 1, 2014
Primary CompletionJan 1, 2020
TodayJul 2, 2026
Enrollment to primary: 6 yearsPosted 12.5 years ago
Interventions
Riluzoledrug