Clinical TrialSuicidalityKetamineCompleted

Sustained Ketamine Effectiveness for Suicidal Ideation (SKESI)

This observational cohort study (n=128) will evaluate the sustained effectiveness of intravenous (IV) ketamine for suicidal ideation in adults experiencing a suicidal crisis due to major depressive disorder.

Target Enrollment
128 participants
Study Type
Phase NA observational
Design
Non-randomized

Detailed Description

This is a retrospective cohort using routinely collected medical records of patients who received IV ketamine infusions for suicidal crisis in the Emergency and Post-Emergency Psychiatric Department at University Hospital Montpellier.

Patients received one or more IV ketamine infusions as an add-on to depression treatment; psychometric assessments and systematic reassessments were performed twice in the month following the last infusion to monitor suicidality and clinical course.

Primary aim is to assess sustained effectiveness on suicidal ideation and behaviour in adults treated between June 2022 and March 2024 (n=128).

Study Protocol

Preparation

sessions

Dosing

sessions

Integration

sessions

Therapeutic Protocol

Manualized psychotherapy included

Study Arms & Interventions

IV ketamine

experimental

Retrospective cohort of patients treated with IV ketamine as part of routine emergency/post-emergency psychiatric care; infusions may be repeated.

Interventions

  • Ketamine
    via IVrepeated

    IV ketamine infusions given as part of routine clinical care; dosing not specified in records.

Participants

Ages
1899
Sexes
Male & Female

Inclusion Criteria

  • Patients treated with IV ketamine in the Psychiatric Emergency and Post-Emergency Department (University Hospital, Montpellier) in context of suicidal crisis
  • Over 18 y.o.

Exclusion Criteria

  • Opposition to data use
  • Subject deprived of liberty (by judicial or administrative decision)
  • Subject protected by law (guardianship or curatorship)
  • Subject not affiliated to a social security system

Study Details

  • Status
    Completed
  • Phase
    Phase NA
  • Type
    observational
  • Design
    Non-randomized
  • Target Enrollment128 participants
  • Timeline
    Start: 2023-12-01
    End: 2024-09-23
  • Compound
  • Topic

Locations

University Hospital, MontpellierMontpellier, France

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