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CompletedNCT00099983

Risperidone Treatment for Military Service Related Chronic PTSD

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

PTSD, Stress Disorders, ...DrugOver 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.

Then choose your country and confirm availability with each study site.

In plain English

Key information made simple

What is this study testing?

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

What would participation involve?

Participants may receive Risperidone, 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.

Your next step

Check the study details

Check the official source, then confirm these points with the research team.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateOctober 2006
Recruitment status
Completed
Enrollment listed in the registry
296
Sponsor
US Department of Veterans Affairs
Sponsor type
Government agency
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
Over 18 Years
Official registry ID
NCT00099983
Official title
CSP #504 - Risperidone Treatment for Military Service Related Chronic Post-Traumatic Stress Disorder

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Study ID: NCT00099983. We help you review the study, but cannot decide medical eligibility.

Check recruitment and locations

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

View official study record (opens in a new tab)

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

United States · 20 sites
  • VA Medical Center, Tuscaloosa
    Tuscaloosa, Alabama
    Site status: Not listed — confirm with the team
  • VA San Diego Healthcare System, San Diego
    San Diego, California
    Site status: Not listed — confirm with the team
  • VA Medical Center, San Francisco
    San Francisco, California
    Site status: Not listed — confirm with the team
  • VA Greater Los Angeles Healthcare System, West LA
    West Los Angeles, California
    Site status: Not listed — confirm with the team
  • VA Connecticut Health Care System (West Haven)
    West Haven, Connecticut
    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
  • Jesse Brown VAMC (WestSide Division)
    Chicago, Illinois
    Site status: Not listed — confirm with the team
  • VA Maryland Health Care System, Baltimore
    Baltimore, Maryland
    Site status: Not listed — confirm with the team
  • VA Medical Center, Jamaica Plain Campus
    Boston, Massachusetts
    Site status: Not listed — confirm with the team
  • VA Medical Center, Minneapolis
    Minneapolis, Minnesota
    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
  • VA Medical Center, Durham
    Durham, 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
  • Ralph H Johnson VA Medical Center, Charleston
    Charleston, South Carolina
    Site status: Not listed — confirm with the team
  • Michael E. DeBakey VA Medical Center (152)
    Houston, Texas
    Site status: Not listed — confirm with the team
  • VA South Texas Health Care System, San Antonio
    San Antonio, Texas
    Site status: Not listed — confirm with the team
  • Central Texas Veterans Health Care System
    Temple, Texas
    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
  • Wlliam S. Middleton Memorial Veterans Hospital, Madison
    Madison, Wisconsin
    Site status: Not listed — confirm with the team
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: The purpose of this research of 400 participants is to determine whether a drug called risperidone can decrease symptoms of Post-Traumatic Stress Disorder (PTSD). It is a placebo-controlled study, meaning that half of the participants will be assigned to receive a pill that. 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 Risperidone, Placebo. Phase 2 studies usually explore whether the intervention may work, while continuing to monitor safety.

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 US Department of Veterans Affairs, which appears to be a government agency. 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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