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CompletedNCT01133301

Naltrexone in the Treatment of Dissociative Symptoms in people with Borderline Personality Disorder

This study is completed. It focuses on personality disorders and currently lists study information in Germany.

Personality disorders, Borderline personality, ...DrugFrom 18 Years to 50 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 Naltrexone may be useful for adults experiencing personality disorders.

What would participation involve?

Participants may receive Naltrexone, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in Germany.

Who is it mainly for?

This study appears to be mainly for adults with personality disorders.

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 dateAugust 1998
Recruitment status
Completed
Enrollment listed in the registry
30
Sponsor
Central Institute of Mental Health, Mannheim
Sponsor type
Research institute
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
Germany
Age range
From 18 Years to 50 Years
Official registry ID
NCT01133301
Official title
Naltrexone in the Treatment of Dissociative Symptoms in Patients With Borderline Personality Disorder

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Recruitment & locations

Completed

Freiburg im Breisgau

Checked Official study record (opens in a new tab)
Registry details
Registry conditions (original wording)

Borderline Personality Disorder; Dissociation

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Central Institute of Mental Health, Mannheim, a research institute.

Does this study involve medication?

Yes. The study involves medication, including Naltrexone and Placebo.

Who can participate?

Listed age limits: 18 years to 50 years.

Is this study still recruiting?

The registry lists this study as completed.

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CompletedEUCTR 2020-003469-20

A double blind, randomized, placebo-controlled, adaptive 14-week Phase IIb trial to evaluate the efficacy and safety of vafidemstat in an adult borderline personality disorder (BPD) population (PORTICO)

This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.