Skip to content

Assessment of effect of intravenous ketamine in suicidal ideas among patients with major depressive disorder in comparison with control group

Assessment of effect of intravenous ketamine in suicidal ideas among patients with major depressive disorder in comparison with control group

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015030921397N1
Enrollment
60
Registered
2015-07-17
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Suicide attempt- Depression. Severe depressive episode without psychotic symptoms, Personal history of self-harm

Interventions

Intervention 1: Intervention group: 0.5 mg/kg IV ketamine/30 min and the patient is monitored for 2, 24, 72 hrs and 7 days for adverse drug reactions. Intervention 2: Control group: 500 cc IV normal s
Treatment - Drugs
Intervention group: 0.5 mg/kg IV ketamine/30 min and the patient is monitored for 2, 24, 72 hrs and 7 days for adverse drug reactions.
Control group: 500 cc IV normal saline as placebo

Sponsors

Vice chancellor for research, Hormozgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: depression diagnosis due to DSM IV criteria; benign major depression episode; suicidal thoughts; no use of antidepression drugs in last month; age above 18 Exclusion criteria: bipolar disorder type 1 & 2; cyclothymia; psychosis having other disorder of 1or 2 axis simultaneusly; drug addiction or withdrawal; medical disease which causes depression; pregnancy; breast feeding; cardiovascular disease history

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The effect of suicidal thoughts. Timepoint: 2, 24, 72 hours and 7 day after drug injection. Method of measurement: Beck suicidal ideation questionnaire.

Secondary

MeasureTime frame
Quantity of depression. Timepoint: 2, 24, 72 hours and 7days after drug injectinon. Method of measurement: Beck depression questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarah Moayedi

Hormozgan University Medical Sciences

Moayedi.f@hums.ac.ir; Famoayedi@gmail.com+98 76 3334 7897

Outcome results

None listed

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