N/A
N=50
Women's Post Traumatic Stress Disorder (PTSD) Research Study
Posttraumatic Stress Disorder
Bottom Line
View on ClinicalTrials.gov: NCT01304940 ↗Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Apr 2019
Primary outcome: Primary: Prepulse Inhibition — -.19; -.31 proportion of change in OEMGR response
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- VA Office of Research and Development
- Primary completion
- Feb 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Prepulse Inhibition |
-.19; -.31 | — |
Summary
The purpose of this study is to examine the relationship between trauma and startle. The investigators are also looking at the effect of menstrual phase on this relationship.
Eligibility Criteria
Inclusion Criteria
- Women, ages 18-55 years old who have a regular menstrual cycle and who can come in to participate in the afternoon
Exclusion Criteria
- Long-term medications, oral or steroid contraceptives, irregular menstrual cycle
Data sourced from ClinicalTrials.gov (NCT01304940). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.