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New drug vs. brain stimulation: which stops suicidal thoughts faster?

NCT ID NCT06355180

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study tested whether a drug called esketamine works as well as electroconvulsive therapy (ECT) for quickly reducing suicidal thoughts in people with depression. 340 adults with major depression or bipolar disorder and active suicidal ideas took part. They received either esketamine infusions or ECT sessions over two weeks, and researchers tracked how many achieved remission of suicidal thoughts.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Esketamine (a fast-acting antidepressant drug)
What this could lead to
If esketamine works as well as ECT, it could offer a less invasive, faster option to reduce suicidal thoughts in people with depression.
What could go wrong
This is a completed trial, but results are not yet published. Esketamine may not be as effective as ECT, and it can cause side effects like dissociation or nausea.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

340 people

The number who actually took part.

Started

Apr 2024

Finished

Aug 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria (all five criteria must be met for an individual to be included): 1. Outpatients or inpatients aged 18 to 65 years (inclusive); 2. Having a current diagnosis of MDD or depressive episode in bipolar I/II disorder, established using the Mini-International Neuropsychiatric Interview, version 7.0.2 (MINI 7.0.2) and according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria; 3. Having a total score of 6 or more on the SSI at screening; 4. Having at least primary school education and the ability to comprehend assessment scales; 5. Having provided written informed consent. Exclusion Criteria (an individual will be excluded if any one of the following criteria is met): 1. Having a current or historical diagnosis of neurodevelopmental, neurocognitive, psychotic, or substance-related disorders according to the DSM-5 criteria; 2. Having active delusions or hallucinations; 3. Suffering from severe/unstable systemic illness (illness affecting the central nervous system, cardiovascular, respiratory, hepatic, renal, endocrine, or hematologic systems) and judged by the investigator as unsuitable for participation; 4. Being judged by the investigator as at risk for substance abuse or addiction; 5. Using reserpine currently; 6. Contraindications to general anesthesia; 7. Having a history of seizure disorders (except for uncomplicated childhood febrile seizures); 8. Having severe drug or food allergies or allergy to any component of the study medication; 9. Having a history of treatment non-response or severe adverse reactions to esketamine, ketamine, or ECT; 10. Having participated in any other clinical trials within the three months before the enrollment; 11. Being pregnant, breastfeeding, or planning to become pregnant (for female participants) or planning to father a child (for male participants) during the study or within 12 weeks after the last dose of medication; 12. Being judged by researchers as unsuitable for participation.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Beijing Anding Hospital

    Beijing, Beijing Municipality, 100088, China

  • Beijing Chaoyang District Third Hospital

    Beijing, China

  • Beijing Daxing District Xinkang Hospital

    Beijing, China

  • Inner Mongolia Autonomous Region Mental Health Center

    Hohhot, China

  • The Second People's Hospital of Dali Bai Autonomous Prefecture

    Dali, China

  • Wuhu Fourth People's Hospital

    Wuhu, Anhui, 241002, China

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