MedPath

The effectiveness of cyproheptadine in the treatment of acute akathisia caused by neuroleptics

Phase 3
Conditions
Akathisia.
Drug induced akathisia
G25.71
Registration Number
IRCT20191218045795N7
Lead Sponsor
Sanandaj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Get antipsychotic
A minimum score of 2 on the akathisia scale BARS

Exclusion Criteria

Receiving beta blocker, mianserin, cyproheptadine, vitamin B6
Suiccidal thoughtsevere
Severe akathisia (score higher than 5 in BARS)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
BARS akathisia score. Timepoint: At the beginning of the study (before the start of the intervention) and 5 days after the start of cyproheptadine. Method of measurement: BARS akathisia questionaire.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath