poisoned patients. F00-F99
Conditions
Interventions
Intervention 1: Intervention group: Diazepam (10 mg) + Haloperidol (5 mg). Intervention 2: Control group: Diazepam (10 mg).
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria include consent to participate in the study, diagnosis of agitation with DSM 5 1 criteria following the consumption of stimulants and age over 18 years.
Exclusion criteria
Exclusion criteria: On the other hand, another set of indicators is considered as exclusion criteria, these exclusion criteria include lack of consent to participate in the study, the presence of risk factors for cognitive disorders such as the presence of brain and nerve diseases (such as seizures, dementia, Parkinson's). ), a history of moderate to severe head trauma, a history of head trauma, decreased level of consciousness, glaucoma, psychosis, moderate to severe dependence on other substances, heart diseases such as long QT 2, and observation of the side effects of the drugs used.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Agitation. Timepoint: 0,10,15,30 min. Method of measurement: richmond questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactPeyman Erfan Talab Evini
Shahid Beheshti University of Medical Sciences
Outcome results
None listed