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Taking people in ItalyPhase 3

Tests ketamine added to electroconvulsive therapy for depression

Tests ketamine with electroconvulsive therapy in adults with treatment-resistant depression.

Key facts

Who runs it
Universita' Vita-salute S. Raffaele
Where
Milan, ItalySee the site
Registry title
The additive effect of ketamine in combination with electroconvulsive stimulation (ECS) in major depressive disorder (MDD): a translational study
Status
Recruiting
Phase
Phase 3
People taking part
30 people, planned
Started
10 Jul 2025
Planned end
31 Aug 2026
Type of study
Interventional
Record updated
2 March 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18-70 with major depressive disorder that has not improved with at least 2 different antidepressants.

Age
18-70 years
Sex
Men and women can join.
Disease stage
Major depressive disorder (diagnosed with the SCID5-CV scale) that is treatment resistant, meaning at least 2 different antidepressants were used without success.
Earlier treatment
At least 2 different antidepressant medicines used without success.

Main reasons for not taking part

  • Chronic neurological disease or intellectual disability
  • Known allergy to ketamine, or any reason ketamine or electroconvulsive therapy is not safe (for example severe heart problems, uncontrolled high blood pressure, stroke in the last 6 months)
  • Alcohol or substance use disorder or substance abuse in the past year
  • Pregnancy or breastfeeding
  • Any other psychiatric disorder besides major depressive disorder

The registry criteria, word for word

Show all 17 criteriaShow less

Who can take part

  • Participant is willing and able to give informed consent for participation in the study
  • Male and Female, aged 18-70
  • Women of childbearing potential (WOCBP) must use at least 1 highly effective method of contraception. Highly effective methods of contraception are those which have a failure rate of <1% (when implemented consistently and correctly) and include: Intrauterine device (IUD), Bilateral tubal ligation, bilateral salpingectomy, or bilateral tubal occlusive procedure, Hormonal contraceptives (eg, oral, patch, or injectable), A double-barrier protection method (eg, condom, sponge, or vaginal diaphragm with spermicide cream, foam, or gel); abstinence from heterosexual intercourse is accepted if this is the participant’s usual lifestyle
  • Diagnosed with major depressive disorder (according to SCID5-CV scale)
  • Affected by treatment resistant depression (defined as at least 2 different antidepressant agents used without success)
  • Adequacy of the score for anesthesia

Who cannot take part

  • Chronic neurological disease
  • Participants with a known hypersensitivity to ketamine or any of its excipients will be excluded from the study
  • Participants with any contraindications to the use of ketamine, such as a history of severe cardiovascular conditions (e.g., uncontrolled hypertension, significant arrhythmias), intracranial hypertension, or severe liver impairment, will also be excluded to prevent potential adverse events
  • Contraindications to the electroconvulsive therapy (severe aortic valve stenosis, implantable cardiac defibrillators, uncontrolled hypertension, clinically significant respiratory, renal or hepatic disease, abdominal aortic aneurysm, endocrine disorders, neuromuscular diseases, space occupying brain lesions, stroke in the last 6 months),
  • Contraindications to the electroconvulsive therapy (severe aortic valve stenosis, implantable cardiac defibrillators, implantable electronic devises, uncontrolled hypertension, clinically significant respiratory, renal or hepatic disease, abdominal aortic aneurism, endocrine disorders, neuromuscular disease, space-occupying brain lesions, stroke in the last 6 months)
  • Patients with Alcohol Use Disorder or Substance Use Disorder or Substance Abuse history in the past year,
  • Cardiovascular conditions
  • Any other Psychiatric Disorders, other than MDD
  • Hepatic impairment
  • Intellectual disability
  • Pregnancy and lactation

Where in Italy

  • Ospedale San Raffaele S.r.l.Milan, ItalyTaking people

About the trial

What the trial wants to find out

The primary objective of this study is to evaluate the antidepressant effect of ketamine in combination with electroconvulsive therapy (ECT) in patients with treatment-resistant depression.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record

Print a page for my doctor

Data and sources

Registry record
Listed on the EU's official list of trials (CTIS).
Official title
The additive effect of ketamine in combination with electroconvulsive stimulation (ECS) in major depressive disorder (MDD): a translational study
Plain-language title
Tests ketamine added to electroconvulsive therapy for depressionGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 9 November 2026.
Record updated
2 March 2026