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UnknownNCT05751525

Sulfonylurea for Neurodevelopmental Disorders; Intellectual Disability; Development Delay; ADHD; Autism Spectrum Disorder; Epilepsy

This study has an unknown status in the United States, in the United Kingdom, in Italy, .... It is testing sulfonylurea for Neurodevelopmental Disorders; Intellectual Disability; Development Delay; ADHD; Autism Spectrum Disorder; Epilepsy.

ADHD, Neurodevelopmental Disorders, ...DrugFrom 2 Years to 50 Years

Current recruitment is not confirmed. Check the official registry or contact the research team before making plans to participate.

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In plain English

Key information made simple

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Your next step

Check the study details

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  • 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

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Study start dateStarted: July 1, 2016
Recruitment status
Unknown
Enrollment listed in the registry
21
Sponsor
Royal Devon and Exeter NHS Foundation Trust
Sponsor type
Non-profit organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Not clearly listed
Locations
United States, United Kingdom, Italy, ...
Age range
From 2 Years to 50 Years
Official registry ID
NCT05751525
Official title
Impact of Timing of Initiation of Sulphonylurea Therapy on Neurodevelopmental Outcomes in Individuals With Intermediate Developmental Delay, Epilepsy and Neonatal Diabetes (iDEND) Syndrome Due to the V59M Mutation in the KCNJ11 Gene

Check recruitment and locations

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

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

Italy · 1 site
  • University of Rome
    Rome
    Site status: Recruiting
    The overall study status does not confirm open recruitment. Check with the team.
Norway · 1 site
  • University of Bergen
    Bergen
    Site status: Recruiting
    The overall study status does not confirm open recruitment. Check with the team.
United Kingdom · 1 site
  • University of Exeter
    Exeter
    Site status: Recruiting
    The overall study status does not confirm open recruitment. Check with the team.
United States · 1 site
  • University of Chicago
    Chicago, Illinois
    Site status: Recruiting
    The overall study status does not confirm open recruitment. Check with the team.

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Study ID: NCT05751525. 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 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 Sulfonylurea. The phase is not clearly listed in the public registry. Phase is mostly relevant for medication studies and some device studies. For this study, it may be more useful to look at what is required, the duration, visits, and eligibility criteria.

Who might this study be for?

This study may concern people with adhd; age range: From 2 Years to 50 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 Royal Devon and Exeter NHS Foundation Trust, which appears to be a non-profit organization. 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?

Current recruitment is not confirmed. Check the official registry or contact the research team before making plans to participate.

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