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CompletedNCT00532493

Cooperative Studies Program #563 - Prazosin and Combat Trauma PTSD

This study is completed. It focuses on PTSD and currently lists study information in the United States.

PTSD, Sleep DisordersDrugOver 18 Years

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

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Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.

Check the official registry

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

United States · 15 sites
  • VA Medical Center, Loma Linda
    Loma Linda, California
    Site status: Not listed — confirm with the team
  • VA Medical Center, Long Beach
    Long Beach, California
    Site status: Not listed — confirm with the team
  • VA Palo Alto Health Care System
    Palo Alto, California
    Site status: Not listed — confirm with the team
  • VA Medical Center, Miami
    Miami, Florida
    Site status: Not listed — confirm with the team
  • Atlanta VA Medical and Rehab Center, Decatur
    Decatur, Georgia
    Site status: Not listed — confirm with the team
  • VA Medical Center, Kansas City MO
    Kansas City, Missouri
    Site status: Not listed — confirm with the team
  • New Mexico VA Health Care System, Albuquerque
    Albuquerque, New Mexico
    Site status: Not listed — confirm with the team
  • New York Harbor HCS
    New York, New York
    Site status: Not listed — confirm with the team
  • VA Medical Center, Durham
    Durham, North Carolina
    Site status: Not listed — confirm with the team
  • Salisbury VAMC
    Salisbury, North Carolina
    Site status: Not listed — confirm with the team
  • VA Medical Center, Providence
    Providence, Rhode Island
    Site status: Not listed — confirm with the team
  • WJB Dorn Veterans Hospital, Columbia
    Columbia, South Carolina
    Site status: Not listed — confirm with the team
  • VA Salt Lake City Health Care System, Salt Lake City
    Salt Lake City, Utah
    Site status: Not listed — confirm with the team
  • VA Puget Sound Health Care System Seattle Division, Seattle, WA
    Seattle, Washington
    Site status: Not listed — confirm with the team
  • Wlliam S. Middleton Memorial Veterans Hospital, Madison
    Madison, Wisconsin
    Site status: Not listed — confirm with the team
In plain English

Key information made simple

What is this study testing?

This study is testing whether prazosin may be useful for adults experiencing ptsd.

What would participation involve?

Participants may receive prazosin, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in the United States.

Who is it mainly for?

This study appears to be mainly for adults with ptsd.

What should you check before joining?

Ask about the dose, safety monitoring, and possible side effects, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

What to expect

Your next step

Study sites are listed in the registry. Recruitment status can differ between sites. Ask the research team to confirm the location, any in-person visits, time commitment, costs or compensation, and participation criteria.

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateStarted: January 6, 2010
Recruitment status
Completed
Enrollment listed in the registry
304
Sponsor
VA Office of Research and Development
Sponsor type
Government agency
Study type
Drug
Intervention type
Medication / drug, OTHER
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
Over 18 Years
Official registry ID
NCT00532493
Official title
CSP #563 - Prazosin and Combat Trauma PTSD (PACT)
Official source
Official registry link

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Study ID: NCT00532493. We help you review the study, but cannot decide medical eligibility.
In practice

For you

Participation may contribute to research. Personal benefit is not guaranteed.

Ask the research team to explain the activities, time commitment, and follow-up involved.

Study sites are listed. Confirm the relevant site and any travel before making plans.

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is this study trying to understand?

Based on the public registry summary, this study is trying to understand: Background: Posttraumatic stress disorder (PTSD) is a debilitating and disabling mental disorder that afflicts at least 25% of Veterans who have suffered life-threatening war zone trauma. Trauma-related nightmares and sleep disturbance are among the most treatment-resistant. The study team can confirm the exact objective and what it means for you.

Does this study involve a medication?

This appears to be a medication / drug study involving prazosin, placebo. Phase 3 studies are usually larger and aim to confirm effectiveness and safety in a broader group.

Who might this study be for?

This study may concern people with ptsd; age range: Over 18 Years. The criteria appear fairly specific, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.

What would I likely need to do?

You may need to take a study treatment and have regular medical follow-up. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.

Will I need to change, stop, or stabilize my current treatment?

The public registry appears to mention rules about current treatment, stability, stopping treatment, or dose changes. Do not change your treatment for a study without medical guidance. Ask the study team and your clinician what is required, what is not allowed, and how safety is monitored.

Will I need to travel or attend in-person visits?

The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.

Who is behind this study?

This study is sponsored by VA Office of Research and Development, which appears to be a government agency. Sponsor website: https://www.research.va.gov. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.

Can I still join this study?

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

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