Moderate brain trauma. S06.2
Conditions
Interventions
Intervention 1: Intervention group: Patients in the citalopram intervention group were prescribed 10 mg per day for the first 3 days, then increased to 20 mg per day. Intervention 2: Control group: Th
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with a consciousness coefficient between 9 and 13 Conscious consent of first -degree companions to enter the study Complete recovery from trauma 4 weeks after the incident Patients with a history of mood disorder must be in complete remission for at least 1 year after discontinuation of treatment
Exclusion criteria
Exclusion criteria: Patients with persistent depression or any other mood disorder based on medical records and doctor's definitive diagnosis Pregnant women or women who plan to become pregnant during the study period Previous history of allergy to Citalopramin Complex and debilitating underlying disease such as cancer, advanced heart failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prevention of depression. Timepoint: One, three and 6 months after the injury. Method of measurement: Glasgow coma scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehdi Shafiei
Esfahan University of Medical Sciences
Outcome results
None listed