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Clinical Trials/NCT01008124
NCT01008124WithdrawnNot Applicable

The Liberatory Maneuver for the Treatment of Benign Paroxysmal Positional Vertigo: A Randomized Controlled Trial

Midwestern University2 sites in 1 countryStarted: November 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
2
Primary Endpoint
Negative Dix-Hallpike maneuver

Study Overview

Brief Summary

This study is being done because the investigators would like to know how effective the Liberatory maneuver is in treating benign paroxysmal positional vertigo (BPPV).

Detailed Description

BPPV is a problem with the inner ear that causes brief periods of vertigo triggered by changes in the position of the head such as rolling, looking up, or bending down. BPPV is presently thought to be caused by small pieces of debris or crystals becoming displaced within the inner ear. It can be treated by moving the patient through a series of positions called a maneuver. There are 2 different maneuvers currently used to treat BPPV by the clinician called the liberatory maneuver and the canalith repositioning procedure. We would like to determine how effective the liberatory maneuver is in the treatment of BPPV compared to a placebo maneuver.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •BPPV involving the posterior canal on only one side

Exclusion Criteria

  • •No other canals involved (anterior canal or lateral canal), no central nervous system disorder, and no other medical condition that would not enable the individual to have the maneuver done.

Arms & Interventions

Liberatory Maneuver

Experimental

Liberatory Maneuver

Intervention: Liberatory Maneuver (Other)

Placebo Maneuver

Placebo Comparator

Placebo Maneuver

Intervention: Placebo maneuver (Other)

Outcomes

Primary Outcomes

Negative Dix-Hallpike maneuver

Time Frame: 1-2 weeks

Secondary Outcomes

  • Self reported willingness to move(1-2 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Janet Odry Helminski, PhD

Dr

Midwestern University

Study Sites (2)

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