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CompletedNCT00094432

Aripiprazole for depression

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

Bipolarity, 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.

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In plain English

Key information made simple

What is this study testing?

This study is testing whether Aripiprazole may be useful for adults experiencing bipolarity.

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 bipolarity.

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 dateJune 2004
Recruitment status
Completed
Enrollment listed in the registry
650
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
NCT00094432
Official title
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of Aripiprazole in the Treatment of Patients With Bipolar I Disorder With a Major Depressive Episode. CN138-146 LT is the 26-week Open Label Extension Phase of the Above Titled Protocol, CN138-146 ST.

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 · 40 sites
  • Local Institution
    Mesa, Arizona
    Site status: Not listed — confirm with the team
  • Local Institution
    La Mesa, California
    Site status: Not listed — confirm with the team
  • Local Institution
    La Palma, California
    Site status: Not listed — confirm with the team
  • Local Institution
    Long Beach, California
    Site status: Not listed — confirm with the team
  • Local Institution
    Redlands, California
    Site status: Not listed — confirm with the team
  • Local Institution
    San Diego, California
    Site status: Not listed — confirm with the team
  • Local Institution
    Sherman Oaks, California
    Site status: Not listed — confirm with the team
  • Local Institution
    Washington D.C., District of Columbia
    Site status: Not listed — confirm with the team
  • Local Institution
    Coral Springs, Florida
    Site status: Not listed — confirm with the team
  • Local Institution
    Jacksonville, Florida
    Site status: Not listed — confirm with the team
  • Local Institution
    St. Petersburg, Florida
    Site status: Not listed — confirm with the team
  • Local Institution
    Marietta, Georgia
    Site status: Not listed — confirm with the team
  • Local Institution
    Edwardsville, Illinois
    Site status: Not listed — confirm with the team
  • Local Institution
    Oak Brook, Illinois
    Site status: Not listed — confirm with the team
  • Local Institution
    Springfield, Illinois
    Site status: Not listed — confirm with the team
  • Local Institution
    Lafayette, Indiana
    Site status: Not listed — confirm with the team
  • Local Institution
    Newton, Kansas
    Site status: Not listed — confirm with the team
  • Local Institution
    New Orleans, Louisiana
    Site status: Not listed — confirm with the team
  • Local Institution
    Shreveport, Louisiana
    Site status: Not listed — confirm with the team
  • Local Institution
    Baltimore, Maryland
    Site status: Not listed — confirm with the team
  • Local Institution
    St Louis, Missouri
    Site status: Not listed — confirm with the team
  • Local Institution
    Clementon, New Jersey
    Site status: Not listed — confirm with the team
  • Local Institution
    Albuquerque, New Mexico
    Site status: Not listed — confirm with the team
  • Local Institution
    Brooklyn, New York
    Site status: Not listed — confirm with the team
  • Local Institution
    Elmsford, New York
    Site status: Not listed — confirm with the team
  • Local Institution
    New York, New York
    Site status: Not listed — confirm with the team
  • Local Institution
    Raleigh, North Carolina
    Site status: Not listed — confirm with the team
  • Local Institution
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • Local Institution
    Media, Pennsylvania
    Site status: Not listed — confirm with the team
  • Local Institution
    Philadelphia, Pennsylvania
    Site status: Not listed — confirm with the team
  • Local Institution
    Pittsburgh, Pennsylvania
    Site status: Not listed — confirm with the team
  • Local Institution
    Columbia, South Carolina
    Site status: Not listed — confirm with the team
  • Local Institution
    DeSoto, Texas
    Site status: Not listed — confirm with the team
  • Local Institution
    Houston, Texas
    Site status: Not listed — confirm with the team
  • Local Institution
    Wichita Falls, Texas
    Site status: Not listed — confirm with the team
  • Local Institution
    Salt Lake City, Utah
    Site status: Not listed — confirm with the team
  • Local Institution
    Charlottesville, Virginia
    Site status: Not listed — confirm with the team
  • Local Institution
    Midlothian, Virginia
    Site status: Not listed — confirm with the team
  • Local Institution
    Bellevue, Washington
    Site status: Not listed — confirm with the team
  • Local Institution
    Charleston, West Virginia
    Site status: Not listed — confirm with the team

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Study ID: NCT00094432. 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 bipolarity. 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, 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 bipolarity; age range: From 18 Years to 65 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.

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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