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treatment of ataxia in patients with acute peripheral vertigo.

Phase 3
Conditions
Acute peripheral vertigo.
Benign paroxysmal vertigo
Registration Number
IRCT2015120722777N2
Lead Sponsor
Vice chancellor for research,Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

aged between 18-60 years old; acute peripheral vertigo and ataxia.
exclusion criteria: history of syncope or cardiac event; considerations of a central origin for vertigo; focal neurological deficits; known pregnancy; evidence of drug-induced vertigo or orthostatic hypotension; known dystonic or adverse reaction to diazepam and promethazine or other similar agents; report of taking medication within 24 hours of ED presentation that might affect the results (e.g., antihistamines, antipsychotics, opioid analgesics or sedatives).

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ataxia. Timepoint: 60 and 120 minutes after intervention. Method of measurement: Romberg Test and tandem gait test.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: 60 and 120 minutes after intervention. Method of measurement: Sphygmomanometer.;Heart Rate. Timepoint: 60 and 120 minutes after intervention. Method of measurement: Pulse oximetry.
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