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Vitamin B6 in the treatment of akathisia

Phase 2
Conditions
medication-induced acute akathisia.
Other extrapyramidal and movement disorders
Registration Number
IRCT201111042935N6
Lead Sponsor
Vice chancellor for research, Kurdistan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
51
Inclusion Criteria

being hospitalized ;receiving neuroleptic
medication; Presence of akathisia based on DSM-IV criteria; Baseline
Barnes Akathisia Scale (BAS) score of at least 2
Exclusion criteria: any hepatic or renal
disease; change in the dose of anticholinergic drugs within 5 days
before the trial; receiving any beta-blocker medication during the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of akathisia. Timepoint: baseline and every day up to 5 days. Method of measurement: Barnes Akathisia Scale (BAS).
Secondary Outcome Measures
NameTimeMethod
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