MedPath

Citalopramin preventing depression in moderate TBI

Phase 3
Conditions
Moderate brain trauma.
S06.2
Diffuse tr
Registration Number
IRCT20221108056446N9
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
300
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath