Study Results
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View full resultsBasic Information
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COMPLETED
PHASE3
38 participants
INTERVENTIONAL
2011-07-31
2013-10-31
Brief Summary
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Detailed Description
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The recommended daily allowance (RDA) for Mg in adults is 4.5 mg/kg; however, all age groups of Americans fall short of the RDA for Mg by 100 mg daily. This lack of appropriate magnesium intake may have negative consequences. For example, the putative Mg mechanism within the auditory system involves a metabolic cellular cascade of events. Specifically, Mg deficiency leads to increased permeability of the calcium channel in the hair cells with a consequent over-influx of calcium, an increased release of glutamate via exocytosis, and overstimulation of N-methyl-D-aspartate receptors on the auditory nerve fibers. Recent studies of both noise-induced hearing loss and idiopathic sensorineural hearing loss have suggested that Mg supplementation may lessen the severity of tinnitus in patients. Mg improved hearing recovery and lessened tinnitus in patients with idiopathic sudden hearing loss. More recently, a well-controlled study that Mg was a relatively safe and convenient adjunct to corticosteroid treatment for enhancing the improvements of hearing in acute-onset sensorineural hearing loss at a dose of 4 g. The protective effect of Mg in noise-induced hearing loss has been previously reported.
Despite these encouraging findings, no controlled study has examined the effect of Mg supplementation for subjects with moderate to severe tinnitus.
In this study subjects made 4 visits to the clinic over about 2 months. At the first visit, subjects had a hearing test. Prior to beginning each round of supplements, subjects were asked to rate the severity of their tinnitus on a 1-10 scale, and to complete the Tinnitus Handicap Inventory (THI) questionnaire. Subjects were then randomized to 1 of 2 groups. One group began with 532 mg of Mg for 25 days, the other group began with a placebo supplement for 25 days.
At visit 2, the subjects had a hearing test, rated their tinnitus, and completed the THI questionnaire as well as the Treatment Period Survey. Subjects did not take any supplement for 2 weeks, then returned for visit 3.
At Visit 3, the subjects had a hearing test, rated their tinnitus, and completed the THI questionnaire they then took the opposite supplement (placebo or Mg) for 25 days.
At Visit 4, the subjects had a hearing test, rated their tinnitus, and completed the THI questionnaire as well as the Treatment Period Survey.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
DOUBLE
Study Groups
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Magnesium first, then placebo
Magnesium 532 mg daily for 25 days followed by 2 weeks of washout followed by 25 days of placebo.
Magnesium
Magnesium 532 mg a day
Placebo
matching form/dosage
Placebo first, then magnesium
Placebo daily for 25 days followed by 2 weeks of washout followed by magnesium 532 mg daily for 25 days.
Magnesium
Magnesium 532 mg a day
Placebo
matching form/dosage
Interventions
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Magnesium
Magnesium 532 mg a day
Placebo
matching form/dosage
Eligibility Criteria
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Inclusion Criteria
* An audiogram within the past 6 months
* Mayo Clinic patients who live in Phoenix area
Exclusion Criteria
* Current treatment with Lithium
* Tinnitus rating with 0, 1, or 2 on the 0-10 Tinnitus scale
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Michael Cevette
Associate Professor of Audiology, College of Medicine
Principal Investigators
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Michael Cevette, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Arizona
Scottsdale, Arizona, United States
Countries
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References
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Cevette MJ, Barrs DM, Patel A, Conroy KP, Sydlowski S, Noble BN, Nelson GA, Stepanek J. Phase 2 study examining magnesium-dependent tinnitus. Int Tinnitus J. 2011;16(2):168-73.
Other Identifiers
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09-008292
Identifier Type: -
Identifier Source: org_study_id
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