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CompletedNCT00105196

Aripiprazole in people with Major Depressive Disorder

This study is completed in the United States. It is testing aripiprazole for depression.

DepressionDrugFrom 18 Years to 65 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 Aripiprazole may be useful for adults experiencing depression.

What would participation involve?

Participants may receive Aripiprazole, 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 depression.

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 dateMarch 2005
Recruitment status
Completed
Enrollment listed in the registry
349
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT00105196
Official title
A Study of Aripiprazole in Patients With Major Depressive Disorder

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 · 34 sites
  • University Of Alabama At Birmingham
    Birmingham, Alabama
    Site status: Not listed — confirm with the team
  • Sharp Mesa Vista Hospital
    San Diego, California
    Site status: Not listed — confirm with the team
  • George Washington University Medical Center
    Washington D.C., District of Columbia
    Site status: Not listed — confirm with the team
  • Cns Clinical Research Group
    Coral Springs, Florida
    Site status: Not listed — confirm with the team
  • Medical College Of Georgia
    Augusta, Georgia
    Site status: Not listed — confirm with the team
  • Carman Research
    Smyrna, Georgia
    Site status: Not listed — confirm with the team
  • Uptown Research Institute, Llc
    Chicago, Illinois
    Site status: Not listed — confirm with the team
  • Cunningham Clinical Research, Llc
    Edwardsville, Illinois
    Site status: Not listed — confirm with the team
  • Comprehensive Neuroscience, Inc.
    Hoffman Estates, Illinois
    Site status: Not listed — confirm with the team
  • Vine Street Clinical Research Center
    Springfield, Illinois
    Site status: Not listed — confirm with the team
  • Clinical Research Institute
    Witchita, Kansas
    Site status: Not listed — confirm with the team
  • Lsu Health Sciences Center
    New Orleans, Louisiana
    Site status: Not listed — confirm with the team
  • Pharmasite Research, Inc.
    Baltimore, Maryland
    Site status: Not listed — confirm with the team
  • Summit Research Network
    Farmington Hills, Michigan
    Site status: Not listed — confirm with the team
  • Summit Research Network
    Flint, Michigan
    Site status: Not listed — confirm with the team
  • University Of Minnesota
    Minneapolis, Minnesota
    Site status: Not listed — confirm with the team
  • Regions Hospital
    Saint Paul, Minnesota
    Site status: Not listed — confirm with the team
  • Radiant Research Las Vegas
    Las Vegas, Nevada
    Site status: Not listed — confirm with the team
  • Behavioral Health Center
    Charlotte, North Carolina
    Site status: Not listed — confirm with the team
  • Midwest Clinical Research Center
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • Phebe Tucker, Md
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Summit Research Network
    Portland, Oregon
    Site status: Not listed — confirm with the team
  • Suburban Research Associates
    Media, Pennsylvania
    Site status: Not listed — confirm with the team
  • University Of Pennsylvania
    Philadelphia, Pennsylvania
    Site status: Not listed — confirm with the team
  • Thomas Jefferson University
    Philadelphia, Pennsylvania
    Site status: Not listed — confirm with the team
  • Southeast Health Consultants
    Charleston, South Carolina
    Site status: Not listed — confirm with the team
  • Usc School Of Medicine
    Columbia, South Carolina
    Site status: Not listed — confirm with the team
  • Community Clinical Research, Inc.
    Austin, Texas
    Site status: Not listed — confirm with the team
  • Radiant Research, Slc
    Salt Lake City, Utah
    Site status: Not listed — confirm with the team
  • University Of Utah School Of Medicine
    Salt Lake City, Utah
    Site status: Not listed — confirm with the team
  • University Of Virginia
    Charlottesville, Virginia
    Site status: Not listed — confirm with the team
  • Northwest Clinical Research Center
    Bellevue, Washington
    Site status: Not listed — confirm with the team
  • Northbrooke Research Center
    Brown Deer, Wisconsin
    Site status: Not listed — confirm with the team
  • Dean Foundation For Health Research & Education
    Middleton, Wisconsin
    Site status: Not listed — confirm with the team

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Study ID: NCT00105196. 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?

This study is exploring medication or study treatment for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.

Does this study involve a medication?

This appears to be a medication / drug study involving Aripiprazole+ ADT, Placebo+ ADT. 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 depression; age range: From 18 Years to 65 Years. The criteria appear fairly broad, 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.

What side effects, interactions, or treatment changes should I check?

If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.

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 Otsuka Pharmaceutical Development & Commercialization, Inc., which appears to be a pharmaceutical company. Sponsor website: https://www.otsuka.co.jp/en/. 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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