Glecaprevir/Pibrentasvir for the Treatment of PTSD
Researchers studied Glecaprevir / Pibrentasvir Pill to find out how it affected post-traumatic stress symptoms in people with PTSD.
Understand this study
What did researchers investigate?
Researchers studied Glecaprevir / Pibrentasvir Pill to find out how it affected post-traumatic stress symptoms in people with PTSD.
Who was this study for?
This study was for people with PTSD. Listed age limits: 19 years to 70 years. Other eligibility criteria applied.
- Listed locations
- White River Junction, United StatesSee all locations and recruitment
- Activities
- Medication described in the protocol
- Compensation
- Payment and expense reimbursement have not been verified.
Study information
- Recruitment status
- Completed
- Enrollment listed in the registry
- 10
- Sponsor
- White River Junction Veterans Affairs Medical Center
- Sponsor type
- Hospital / academic medical center
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 2, Phase 3This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
- Locations
- United States
- Age range
- From 19 Years to 70 Years
- Official registry ID
- NCT05446857
- Official title
Show the full official title
Glecaprevir/Pibrentasvir for the Treatment of PTSD
Recruitment & locations
CompletedWhite River Junction
Questions about this study
What did researchers investigate?
Researchers studied Glecaprevir / Pibrentasvir Pill to find out how it affected post-traumatic stress symptoms in people with PTSD.
Who is behind this study?
The study sponsor is White River Junction Veterans Affairs Medical Center, a hospital or academic medical center.
Did this study involve medication?
Yes. The study involved medication, including Glecaprevir / Pibrentasvir Pill.
Who was this study for?
This study was for people with PTSD. Listed age limits: 19 years to 70 years. Other eligibility criteria applied.
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