Add-on Buprenorphine at Analgesic Doses for the Treatment of Severe Suicidal Ideas During a Major Depressive Episode

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-65
SponsorCentre Hospitalier Universitaire de Nīmes

About this trial

This study aims at investigating if adjunctive buprenorphine at low dose to treatment as usual is effective in reducing severe suicidal ideas in major depressive episode, and at determining the most effective dose.

Eligibility criteria

Qualifiers

The patient has been correctly informed.

The patient must have given his/her informed and signed the consent form.

The patient must be insured or beneficiary of a health insurance plan.

The patient is at least 18 years old and 65 years old at the most.

Disqualifiers

The patient is participating in another interventional trial;

The patient is in an exclusion period determined by a previous study;

The patient is under judicial protection, or is an adult under guardianship;

The patient is under compulsory admission;

Trial design

Treatments tested in this trial

  • Buprenorphine
  • Placebo

Treatment groups

180 Participants
are divided into 3 treatment groups