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Observation of the effect of esketamine rapid antidepressant in patients with different ages

Observation of the effect of esketamine rapid antidepressant in patients with different ages

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129132
Enrollment
Unknown
Registered
2026-07-31
Start date
2024-11-08
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression disorder

Interventions

Adolescent group:Esketamine 0.2mg/kg was infused by a peripheral intravenous pump
The middle and elderly group:Esketamine 0.2mg/kg was infused by a peripheral intravenous pump

Sponsors

Changzhou Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Depressive disorder without psychotic symptoms was diagnosed clinically by a licensed psychiatrist and met the Diagnostic and Statistical Manual of Mental Disorders, Fifth edition (DSM-5); 2.The total score of Montgomery Depression Scale (MADRS) was 22 or higher; 3.Understand the content of the study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Patients with other severe mental disorders conforming to DSM-5 diagnostic criteria, including schizophrenia, schizoaffective disorder, bipolar disorder, etc; 2.History of severe physical or brain organic diseases, traumatic brain injury and epilepsy; 3.History of drug, alcohol, or other psychoactive substance abuse; 4.Having metal in the body, such as a pacemaker or electrodes in the brain; 5.Previous history of allergy to anesthetics; 6.Women who are pregnant or breastfeeding or who plan to become pregnant; 7.Patients with contraindications of magnetic resonance imaging scanning or factors affecting imaging quality, such as cardiac pacemaker, cardiovascular and cerebrovascular metal stents, cochlear implants, metal dentures, etc; 8.Other conditions deemed inappropriate by the investigator;

Design outcomes

Primary

MeasureTime frame
Montgomery Depression Scale;

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index scale;Sleep monitoring;

Countries

China

Contacts

Public ContactWu Zhouquan

Changzhou Second People's Hospital

151897127@qq.com+86 519 8813 2395

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026