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Efficacy of ketamine in the treatment of refractory depression

Efficacy of ketamine in the treatment of refractory depression

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043131
Enrollment
Unknown
Registered
2021-02-05
Start date
2021-02-13
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

refractory depression

Interventions

experimental group:Dilute Ketamine 0.25mg/kg in 50ml of 0.9% saline solution, and administer it slowly through intravenous infusion over 40 minutes, 3 times a week for 2 weeks, 6 times in total.

Sponsors

Zhongda Hospital, School of Medicine, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18~60 years; 2. Right-handed; 3. Meet the DSM-5 and CCMD-3 diagnostic criteria for MDD; 4. Current course of disease (last onset) at least 2 weeks; 5. HAMD-24 score >= 18 points; 6. No clinical remission standard (HAMD reduction rate < 50%) was achieved after receiving at least two antidepressant treatments since onset. 7. No electroconvulsive therapy was received within half a year before inclusion.

Exclusion criteria

Exclusion criteria: 1. Comorbid another mental illness; 2. Have a history of alcohol/drug dependence or smoke > 10 per day; 3. Serious physical diseases of the heart, liver, kidney, brain and hematopoietic system, central nervous system infection, skull injury, epilepsy, multiple sclerosis, toxic metabolic disease, Parkinson's disease or intracranial tumors; 4. Family history of hereditary diseases; 5. Endocrine system diseases such as diabetes, hyperthyroidism or hypothyroidism; 6. Patients with suicidal intention.

Design outcomes

Primary

MeasureTime frame
HAMD reduction rate;treatment emergent symptom scale;

Countries

China

Contacts

Public ContactYonggui Yuan

Zhongda Hospital, School of Medicine, Southeast University

yygylh2000@sina.com+86 139 1393 9082

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026