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CompletedNCT05877807

Effect of Baclofen to Prevent PTSD: 5 Years Follow-up of the BACLOREA study

This study is completed in France. It is testing baclofen for PTSD.

PTSD, AlcoholismDrugFrom 18 Years to 80 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 Baclofen may be useful for adults experiencing ptsd.

What would participation involve?

Participants may receive Baclofen, complete questionnaires or follow-up assessments, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in France.

Who is it mainly for?

This study appears to be mainly for adults with ptsd.

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 dateStarted: September 3, 2023
Recruitment status
Completed
Enrollment listed in the registry
94
Sponsor
Nantes University Hospital
Sponsor type
Hospital / academic medical center
Study type
Drug
Intervention type
Medication / drug, OTHER
Study phase
Not clearly listed
Locations
France
Age range
From 18 Years to 80 Years
Official registry ID
NCT05877807
Official title
Effect of Baclofen to Prevent Post-Traumatic Stress Disorder: 5 Years Follow-up of the BACLOREA Randomized Trial

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.

France · 13 sites
  • Brest University Hospital
    Brest, Finistère
    Site status: Not listed — confirm with the team
  • Cornouaille Hospital
    Quimper, Finistère
    Site status: Not listed — confirm with the team
  • Montpellier University Hospital
    Montpellier, Hérault
    Site status: Not listed — confirm with the team
  • Rennes University Hospital
    Rennes, Ile-et-Vilaine
    Site status: Not listed — confirm with the team
  • Tours University Hospital
    Tours, Indre-et-Loire
    Site status: Not listed — confirm with the team
  • Nantes University Hospital
    Nantes, Loire-Atlantique
    Site status: Not listed — confirm with the team
  • Saint-Nazaire Hospital
    Saint-Nazaire, Loire-Atlantique
    Site status: Not listed — confirm with the team
  • Angers University Hospital
    Angers, Maine-et-Loire
    Site status: Not listed — confirm with the team
  • South Bretagne Hospital Center
    Lorient, Morbihan
    Site status: Not listed — confirm with the team
  • Le Mans University Hospital
    Le Mans, Sarthe
    Site status: Not listed — confirm with the team
  • Vendee Departmental Hospital
    La Roche-sur-Yon, Vendee
    Site status: Not listed — confirm with the team
  • Poitiers University Hospital
    Poitiers, Vienne
    Site status: Not listed — confirm with the team
  • Saint-Antoine Hospital (AP-HP)
    Paris, Île-de-France Region
    Site status: Not listed — confirm with the team

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Study ID: NCT05877807. 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?

Based on the public registry summary, this study is trying to understand: Considering the results of the Baclorea study (10% reduction in episodes of agitation in intensive care in the Baclofen group), the investigators would like to know whether this reduction in agitation also results in a reduction in the incidence of the syndrome of long-term. The study team can confirm the exact objective and what it means for you.

Does this study involve a medication?

This appears to be a medication / drug study involving Baclofen, Placebo. 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 ptsd; age range: From 18 Years to 80 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 Nantes University Hospital, which appears to be a hospital or academic medical center. 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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