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TerminatedNCT04507204

Effectiveness of Adhansia XR in ADHD

This study was terminated in the United States. It is testing Adhansia XR for ADHD.

ADHDDrugOver 12 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 Real-World Evidence of Duration of Effect of Adhansia XR may be useful for adolescents experiencing ADHD.

What would participation involve?

Participants may receive Real-World Evidence of Duration of Effect of Adhansia XR, attend study visits with the research team. The registry lists locations in the United States.

Who is it mainly for?

This study appears to be mainly for adolescents with ADHD. Because it involves minors, a parent or guardian may need to be involved.

What should you check before joining?

Ask about the dose, safety monitoring, and possible side effects, whether there is a comparison group, how many visits or travel steps are needed, what role parents or guardians have in the process.

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 dateStarted: July 30, 2020
Recruitment status
Terminated
Enrollment listed in the registry
267
Sponsor
Purdue Pharma LP
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
Over 12 Years
Official registry ID
NCT04507204
Official title
Real-world Evidence of Duration of Adhansia XR for Treatment of ADHD (RE-DAX): An Open-label Pragmatic Study to Assess the Real-world Effectiveness of Adhansia XR in Treatment of Adult and Adolescent Patients With ADHD in the United States

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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 · 35 sites
  • Harmonex, Inc.
    Dothan, Alabama
    Site status: Not listed — confirm with the team
  • Southern California Research LLC
    Beverly Hills, California
    Site status: Not listed — confirm with the team
  • CT Clinical Research
    Cromwell, Connecticut
    Site status: Not listed — confirm with the team
  • Gulfcoast Clinical Research Center
    Fort Myers, Florida
    Site status: Not listed — confirm with the team
  • Reliable Clinical Research, LLC
    Hialeah, Florida
    Site status: Not listed — confirm with the team
  • Eastern Research. Inc.
    Hialeah, Florida
    Site status: Not listed — confirm with the team
  • Wellness Research Center Inc.
    Miami, Florida
    Site status: Not listed — confirm with the team
  • AdventHealth Medical Group Pediatrics at Orange City
    Orange City, Florida
    Site status: Not listed — confirm with the team
  • Pediatric Epilepsy & Neurology Specialists
    Tampa, Florida
    Site status: Not listed — confirm with the team
  • Clinical Integrative Research Center of Atlanta
    Atlanta, Georgia
    Site status: Not listed — confirm with the team
  • Revive Research Institute
    Elgin, Illinois
    Site status: Not listed — confirm with the team
  • AMR-Baber Research Inc.
    Naperville, Illinois
    Site status: Not listed — confirm with the team
  • BTC of New Bedford, LLC
    New Bedford, Massachusetts
    Site status: Not listed — confirm with the team
  • Neurobehavioral Medicine Group
    Bloomfield Hills, Michigan
    Site status: Not listed — confirm with the team
  • Rochester Center for Behavioral Medicine
    Rochester Hills, Michigan
    Site status: Not listed — confirm with the team
  • Psychiatric Care and Research Center
    O'Fallon, Missouri
    Site status: Not listed — confirm with the team
  • St. Charles Psychiatric Associates - Midwest Research Group
    Saint Charles, Missouri
    Site status: Not listed — confirm with the team
  • Clinical Research of Southern Nevada, LLC
    Las Vegas, Nevada
    Site status: Not listed — confirm with the team
  • Center for Emotional Fitness
    Cherry Hill, New Jersey
    Site status: Not listed — confirm with the team
  • Bioscience Research, LLC
    Mount Kisco, New York
    Site status: Not listed — confirm with the team
  • Icahn School of Medicine at Mount Sinai
    New York, New York
    Site status: Not listed — confirm with the team
  • Richmond Behavioral Associates
    Staten Island, New York
    Site status: Not listed — confirm with the team
  • Duke University Medical Center
    Durham, North Carolina
    Site status: Not listed — confirm with the team
  • Mid-Ohio Behavioral Health
    Columbus, Ohio
    Site status: Not listed — confirm with the team
  • SFM Clinical Trials
    Scotland, Pennsylvania
    Site status: Not listed — confirm with the team
  • Rainbow Research
    Barnwell, South Carolina
    Site status: Not listed — confirm with the team
  • FutureSearch Trials of Dallas, LP
    Dallas, Texas
    Site status: Not listed — confirm with the team
  • InSite Clinical Research, LLC
    DeSoto, Texas
    Site status: Not listed — confirm with the team
  • Red Oak Psychiatry Associates, PA
    Houston, Texas
    Site status: Not listed — confirm with the team
  • Road Runner Research, Ltd.
    San Antonio, Texas
    Site status: Not listed — confirm with the team
  • Family Psychiatry of the Woodlands
    The Woodlands, Texas
    Site status: Not listed — confirm with the team
  • Dixie Pediatrics
    St. George, Utah
    Site status: Not listed — confirm with the team
  • Clinical Research Partners, LLC
    Petersburg, Virginia
    Site status: Not listed — confirm with the team
  • Eastside Therapeutic Resource Inc dba Core Clinical Research
    Everett, Washington
    Site status: Not listed — confirm with the team
  • MultiCare Health System - Rockwood Clinic
    Spokane, Washington
    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?

This study is exploring medication or study treatment for people with adhd. 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 Adhansia XR, Concerta. Phase 4 studies usually happen after treatment approval, to monitor real-world use.

Who might this study be for?

This study may concern people with adhd; age range: Over 12 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 Purdue Pharma LP, which appears to be a pharmaceutical company. 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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