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The Liberatory Maneuver for the Treatment of Benign Paroxysmal Positional Vertigo (BPPV)

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

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01008124
Acronym
LM_BPPV
Enrollment
0
Registered
2009-11-05
Start date
2009-11-30
Completion date
2010-11-30
Last updated
2021-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vertigo, Vestibular Disease

Keywords

Benign Paroxysmal Positional Vertigo, BPPV, PC, BPPN, Vertigo

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.

Interventions

OTHERLiberatory Maneuver

3 cycles of the liberatory maneuver initial session.

3 cycles placebo maneuver initial session.

Sponsors

Northwestern University
CollaboratorOTHER
Midwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frame
Negative Dix-Hallpike maneuver1-2 weeks

Secondary

MeasureTime frame
Self reported willingness to move1-2 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026