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CompletedNCT01818895

Terminal Weaning of Mechanical Ventilation or Extubation in Anticipation of Death in the Intensive Care Unit: Impact on Relatives, Care Givers and the Dying Process - A Prospective, Observational Study

This study is completed in France. It focuses on Withdrawal; Anxiety; Depression; PTSD.

PTSD, Depression, ...ObservationalOver 18 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 observational study follows adults living with ptsd to understand their experience, outcomes, or changes over time.

What would participation involve?

Participants may answer questionnaires, join interviews, or provide follow-up information, attend study visits with the research team. 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 whether there is 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 dateApril 2013
Recruitment status
Completed
Enrollment listed in the registry
458
Sponsor
Centre Hospitalier Departemental Vendee
Sponsor type
Unknown or unclear
Study type
Observational
Intervention type
Interview / survey / observational
Study phase
Not clearly listed
Locations
France
Age range
Over 18 Years
Official registry ID
NCT01818895
Official title
Terminal Weaning of Mechanical Ventilation or Extubation in Anticipation of Death in the Intensive Care Unit: Impact on Relatives, Care Givers and the Dying Process - A Prospective, Multicenter, Observational Study

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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.

France · 44 sites
  • Réanimation médicale CHU
    Angers
    Site status: Not listed — confirm with the team
  • Réanimation, CH d'Angoulême
    Angoulême
    Site status: Not listed — confirm with the team
  • Réanimation, CH d'Annecy
    Annecy
    Site status: Not listed — confirm with the team
  • Réanimation
    Belfort
    Site status: Not listed — confirm with the team
  • CHU Pellegrin Tripode
    Bordeaux
    Site status: Not listed — confirm with the team
  • Réanimation, CHU
    Bordeaux
    Site status: Not listed — confirm with the team
  • CHU Ambroise Paré
    Boulogne
    Site status: Not listed — confirm with the team
  • CHU La Cavale Blanche
    Brest
    Site status: Not listed — confirm with the team
  • CHU de Côte de Lumière
    Caen
    Site status: Not listed — confirm with the team
  • Centre Hospitalier, Service de réanimation
    Charleville-Mézières
    Site status: Not listed — confirm with the team
  • CH de Chartres
    Chartres
    Site status: Not listed — confirm with the team
  • CHU Gabriel Montpied, Clermont Ferrand
    Clermont-Ferrand
    Site status: Not listed — confirm with the team
  • CHU Louis Mourier
    Colombes
    Site status: Not listed — confirm with the team
  • CH de Dieppe
    Dieppe
    Site status: Not listed — confirm with the team
  • CHU Dijon
    Dijon
    Site status: Not listed — confirm with the team
  • CHU Raymond Poincaré
    Garches
    Site status: Not listed — confirm with the team
  • CHU Grenoble
    Grenoble
    Site status: Not listed — confirm with the team
  • CHD de la Vendée
    La Roche-sur-Yon
    Site status: Not listed — confirm with the team
  • CH de La Rochelle
    La Rochelle
    Site status: Not listed — confirm with the team
  • CH du Mans
    Le Mans
    Site status: Not listed — confirm with the team
  • CH du Puy
    Le Puy-en-Velay
    Site status: Not listed — confirm with the team
  • CH Docteur Schaffner
    Lens
    Site status: Not listed — confirm with the team
  • CHU de Lille
    Lille
    Site status: Not listed — confirm with the team
  • CH de Lorient
    Lorient
    Site status: Not listed — confirm with the team
  • CHU Marseille, Hopital La Timone
    Marseille
    Site status: Not listed — confirm with the team
  • CHU de Marseille, Hopital Nord
    Marseille
    Site status: Not listed — confirm with the team
  • CH Marc Jacquet
    Melun
    Site status: Not listed — confirm with the team
  • CH de Montauban
    Montauban
    Site status: Not listed — confirm with the team
  • CHI André Grégoire
    Montreuil
    Site status: Not listed — confirm with the team
  • CH de Mulhouse
    Mulhouse
    Site status: Not listed — confirm with the team
  • CHU de Nantes - Hôtel Dieu
    Nantes
    Site status: Not listed — confirm with the team
  • CHU Orléans - Réanimation Médicale
    Orléans
    Site status: Not listed — confirm with the team
  • CHU Saint Louis
    Paris
    Site status: Not listed — confirm with the team
  • CHU Paris Cochin
    Paris
    Site status: Not listed — confirm with the team
  • Groupe Hospitalier Paris Saint Joseph
    Paris
    Site status: Not listed — confirm with the team
  • CHU Hopital Européen Georges Pompidou
    Paris
    Site status: Not listed — confirm with the team
  • CHU Lariboisière
    Paris
    Site status: Not listed — confirm with the team
  • CHU Poitiers
    Poitiers
    Site status: Not listed — confirm with the team
  • CH de Roanne
    Roanne
    Site status: Not listed — confirm with the team
  • Hôpital Delafontaine
    Saint-Denis
    Site status: Not listed — confirm with the team
  • CH de Saint-Nazaire
    Saint-Nazaire
    Site status: Not listed — confirm with the team
  • Hôpital Foch
    Suresnes
    Site status: Not listed — confirm with the team
  • CHU Tours
    Tours
    Site status: Not listed — confirm with the team
  • Institut Gustave Roussy
    Villejuif
    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?

Based on the public registry summary, this study is trying to understand: The purpose of the study is to assess the dying process in critically ill patients with decision to withdraw invasive mechanical ventilation in anticipation of death and to compare effects of extubation and those of terminal weaning of mechanical ventilation on relatives and. The study team can confirm the exact objective and what it means for you.

Is this an interview, survey, or observational study?

This appears to be a interview / survey / observational study. Phase is mainly useful to check for medication studies and some device studies.

Who might this study be for?

This study may concern people with ptsd; age range: Over 18 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 answer questionnaires or take part in interviews. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.

Could the questions feel emotionally difficult or personal?

If the study involves interviews or questionnaires, some questions may feel personal or emotionally sensitive. Ask whether you can skip questions, pause, stop, and how your answers will be protected. 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 Centre Hospitalier Departemental Vendee, which appears to be unknown or unclear. 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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