Skip to content
CompletedPhase 3

Effects of Ketamine in the Acute Phase of Suicidal Ideation

NCT02299440 · KETIS · Centre Hospitalier Universitaire de Nīmes

Closed to entry
Status
Not accepting participants
Phase 3
Phase
156
Target enrolment
9
Study sites
Outside the US

What it is testing

Summary

The primary objective of this study is to assess the efficacy of ketamine versus a placebo for the short-term (at 72h, i.e. 24h after the last perfusion) relief of suicidal ideation, measured using the BSS hetero questionnaire, in patients hospitalized for suicide risk.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • BSSI score

    Measured over Day 3

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * French speaking patients freely hospitalized for prevention of suicide and who have a medium or high suicide risk score according to a MINI structured interview * The patient is able to understand how the study is carried out and the tests performed * The patient is deemed capable of giving his/her informed consent * The patient has been correctly informed * The patient must have given his/her informed and signed consent. * The patient must be insured or beneficiary of a health insurance plan. * Presence of suicidal ideation according to the SSI score (score \> 3) * Negative pregnancy test for women of childbearing age Exclusion Criteria: * The patient is participating in another interventional study * Within the past three months, the patient has participated in another interventional study * The patient is in an exclusion period determined by a previous study * The patient is under judicial protection * The patient is an adult under guardianship * The patient refuses to sign the consent * The patient is not able to understand the informed consent * Pregnancy or breastfeeding * History of schizophrenia or other psychotic disorders * Presence of psychotic symptoms at initial interview * Schizoid or schizotypic personality disorder * Positive urine screening for illicit substances, excluding cannabis * Substance dependence in the preceding month (excluding nicotine or caffeine) * Concomitant treatment with electroconvulsive therapy * Unstable somatic pathology * Clinically significant anomalies found during clinical examination, biological test or ECG * Non-stabilized hypertension or hypertension \> 180/100 * Known or suspected contra-indication for ketamine (includes interactions): hypersensitivity to ketamine, hypertension, class IV cardiac insufficiency, history of stroke, hepatic or cutaneous porphyria, history of intracranial hypertension

Where

9 study sites

FacilityCityRegionCountry
CHU de Clermont Ferrand - Hôpital Gabriel-MontpiedClermont-FerrandFrance
CHRU de Lille - Hôpital Michel FontanLilleFrance
CHRU de Montpellier - Hôpital LapeyronieMontpellierFrance
Clinique Les SophorasNîmesFrance
CHRU de Nîmes - Hôpital Universitaire CarémeauNîmesFrance
APHP - Hôpital LariboisièreParisFrance
Centre Hospitalier Sainte-AnneParisFrance
CMME Centre Hospitalier Sainte AnneParisFrance
CHRU de Tours - Clinique Psychiatrique UniversitaireSaint-Cyr-sur-LoireFrance

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT02299440 on ClinicalTrials.gov →

Last updated in the registry 2025-12-01. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits