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The Effect of Ketamine on Control of Aggressive Patients

Comparison of Intramuscular Ketamine versus Haloperidol in Control of Aggressive Patients in Emergency Department

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180129038549N5
Enrollment
90
Registered
2018-04-21
Start date
2015-11-22
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Agitated Patients. Violent behavior

Interventions

Intervention 1: Intervention group: Ketamine 4mg/kg (50 mg/ml, made in ROTEXMEDICA Co.). If aggression is not controlled the second dose is injected in half of the initial dose(2mg/kg). If is not yet

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All the patients who intended to damage themselves or others Altered mental status score (AMSS) +2 or +3 Required physical restraint and parenteral sedation

Exclusion criteria

Exclusion criteria: serious physical illness History of heart disease pregnancy drug dependence treatment with a benzodiazepine or neuroleptic within the previous 24 hours Ketamine and Haloperidol contraindications

Design outcomes

Primary

MeasureTime frame
Aggression control. Timepoint: Every 5 minutes. Method of measurement: altered mental status score.

Secondary

MeasureTime frame
Side effects. Timepoint: Every 15 minutes. Method of measurement: Physical exam.;Frequency of repeat dosing. Timepoint: After 6 hour. Method of measurement: Physical exam.;Vital signs. Timepoint: Every 5 minutes. Method of measurement: Physical exam.;Satisfaction. Timepoint: After 6 hour. Method of measurement: Questionnaire.;Intubation. Timepoint: After 6 hour. Method of measurement: Counts.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarhad Heydari

Esfahan University of Medical Sciences

drfarhadheydari@gmail.com+98 31 3620 2020

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 23, 2026