HC-BPPV Clinical Trial
— BPPV-HCOfficial title:
Randomized Multicenter Study of Treatment of Horizontal Canal Benign Paroxysmal Positional Vertigo
Verified date | May 2011 |
Source | Chonbuk National University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Food and Drug Administration |
Study type | Interventional |
The purpose of this study was to compare the immediate efficacies of each treatment maneuvers in treatment of apogeotropic horizontal canal benign paroxysmal positional vertigo (HC-BPPV).
Status | Completed |
Enrollment | 157 |
Est. completion date | May 2011 |
Est. primary completion date | May 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - a history of brief episodes of positional vertigo, - direction-changing horizontal nystagmus beating toward the uppermost (apogeotropic nystagmus) or undermost (geotropic nystagmus) ear in both the lateral head turning positions, - no spontaneous nystagmus during upright sitting position, and - absence of identifiable central nervous system disorders that could explain the positional vertigo and nystagmus. Exclusion Criteria: - central positional nystagmus with identifiable CNS lesions that could explain the positional nystagmus |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Chonbuk National University Hospital | Jeonju | Cholabuk-do |
Korea, Republic of | Seoul National University Bundang Hospital | Seongnam | Kyoungki-do |
Lead Sponsor | Collaborator |
---|---|
Chonbuk National University | Seoul National University Bundang Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Treatment of Apogeotropic Horizontal Canal Benign Paroxysmal Positional Vertigo: A Randomized Clinical Trial | The immediate treatment response was determined by participating neurologists in each clinic without knowing the maneuver applied to each patient from 30 minutes to one hour after initial maneuver. The absence of both vertigo and nystagmus was required to determine a resolution. | one hour | No |