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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00182273 |
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Date of registration:
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13/09/2005 |
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Primary sponsor: |
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Public title:
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Canalith Repositioning Procedure for BPPV in Primary Care
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Scientific title:
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Treatment of Benign Paroxysmal Positional Vertigo With the Canalith Repositioning Procedure in Family Practice: A Randomized Controlled Trial |
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Date of first enrolment:
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January 2002 |
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Target sample size:
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56 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00182273 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
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Countries of recruitment
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Canada
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Contacts
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Name:
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Juan Munoz, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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McMaster University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- confirmed BPPV by positive Dix-Hallpike test
Exclusion Criteria:
- · Positive results of the Dix-Hallpike maneuver in both right and left head-hanging
position;
- Evidence of ongoing central nervous system disease (e.g., transient ischemic
attack);
- Otitis media;
- Osteosclerosis;
- Inability to tolerate a diagnostic Dix-Hallpike head-hanging maneuver;
- Severe degenerative disc disease of cervical spine;
- Severe and uncontrolled angina or hypertension
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Benign Paroxysmal Positional Vertigo
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Intervention(s)
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Procedure: Canalith repositioning maneuver (CRM)
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Primary Outcome(s)
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Self-reported resolution (affirmative response to question: “Do you feel that the dizziness has completely resolved?”) of vertigo and/or a negative result of the Dix-Hallpike maneuver
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Secondary Outcome(s)
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Duration of cure, relapse rates
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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