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?Antidepressant effect of ketamine

Comparison of anti-depressant effect of oral ketamine, intramuscular ketamine and electroconvulsive therapy in the patients with major depressive disorder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090801002266N8
Enrollment
45
Registered
2018-10-31
Start date
2018-10-12
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

Major depressive disorder. Major depressive disorder, recurrent severe without psychotic features

Interventions

Intervention 1: First intervention group: intra muscular ketamine, NMDA antagonist, 0.5mg/kg dosage, 500 mg vial, rotex medica factory in Germany, 6-9 injection through 3weeks. Intervention 2: Second

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Major depressive patients based on DSM 5 criteria candidate for electro convulsive therapy Age between 18-70 years old Informed consent form obtained

Exclusion criteria

Exclusion criteria: Drug side effects which discontinuation is necessary Patient`s disagreement to stay in study Deterioration of patient`s symptoms Not to respond after 4 intervention sessions. Drug sensitivity Severe or active hepatic renal cardiac urological disease Substance abuse Previous manic or hypo manic episode Catatonia Secondary depression due to another medical conditions History of psychosis

Design outcomes

Primary

MeasureTime frame
Depression score in hamilton depression scale. Timepoint: Before intervention, 24 hours, one week, two weeks, three weeks, four weeks and eight weeks after begining the intervention. Method of measurement: Hamilton depression scale-17 items.

Secondary

MeasureTime frame
Suicidal scores in beck scale for suicidal ideation. Timepoint: Before intervention, 24 hours, one week, two weeks, three weeks, four weeks and eight weeks after begining the intervention. Method of measurement: Beck scale for sicidal ideation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Kheirabadi

Esfahan University of Medical Sciences

kheirabadi@bsrc.mui.ac.ir+98 31 3222 2135

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026