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TerminatedPhase 2

Study of Depression-Ketamine-Brain Function

NCT01135758 · Markus KOSEL

Closed to entry
Status
Not accepting participants
Phase 2
Phase
10
Target enrolment
1
Study sites
Outside the US

What it is testing

Summary

Targeting the glutamatergic system to treat depression is a new and promising strategy based on studies at the molecular, synaptic, and neuronal level but also on results of studies conducted in animal models and first clinical studies involving depressed patients.Ketamine has been proposed as a novel approach to induce rapid antidepressant response. In this pilot project the investigators aim to introduce this novel and promising approach into clinical practice. Besides the assessment of clinical efficacy, the investigators will put a special emphasis on the assessment of ketamine-associated effects on brain function using fMRI and cognitive testing.

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

  • Difference of the MADRS score at baseline and after ketamine injection

    Measured over 40, 80, 110, 230 min, 1, 2, 3, 6, 7, 10 d after ketamine administration

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 to 65 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Men and women aged 18 to 65 years with a diagnosis of major depressive disorder without psychotic features. * Drug-resistant depressed patients (defined as non-response to two sufficiently long (at least 6 weeks) drug trials at the maximal authorized or tolerated dose) * Score 25 or higher on the Montgomery-Asberg Depression Rating Scale * Stable psychotropic medication (antidepressants, antipsychotics, mood stabilizers) during the last 6 weeks prior to inclusion. * Legally competent subjects agreeing to comply with the requirements of the study and authorizing the transmission of relevant information to competent physicians in the case of a clinically relevant previously unknown finding during an MRI examination. Exclusion Criteria: * Subjects with co-morbid substance abuse or dependence during the 3 months prior to inclusion, except nicotine consumption. * Patients judged to be at serious suicide risk (score ≥ 4 at item 10 of the MADRS). * Patients with any other DSM-IV axis one diagnosis including bipolar disorder except for anxiety disorder which are not dominating the clinical presentation. * History of antidepressant or substance-induced hypomania or mania. * History of psychotic symptoms. * Patients with any contra-indication to the administration of ketamine, especially present diagnosis or antecedents of clinically relevant cardiovascular disorders (clinically significant or not adequately treated hypertension, present or previous diagnosis of cardiovascular disorder such as stroke or heart attack etc). * Any MRI contraindication, especially metallic implants, pacemaker, etc. * Pregnant women, breast-feeding women, women of childbearing age without effective means of contraception. * Treatment during the last 2 weeks with thyroid hormones and sympathicomimetic drug. * Present or past diagnosis of eclampsia or preeclampsia. * Untreated or insufficiently treated hyperthyroidism. * Known hypersensitivity to ketamine or to the excipient (benzethonium chloride). * Present or past diagnosis of glaucoma, intracranial hypertension.

Where

1 study site

FacilityCityRegionCountry
Service de Psychiatrie Adulte, Programme dépressionGenevaSwitzerland

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.

NCT01135758 on ClinicalTrials.gov →

Last updated in the registry 2015-12-07. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits

Substance