A Clinical Trial of the Optimal Treatment Period and Long-term Efficacy of Functional Electrical Stimulation (FES) on Sleep Bruxism
NCT ID: NCT01000389
Last Updated: 2011-06-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
23 participants
INTERVENTIONAL
2009-10-31
2011-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Grindcare® (Biofeedback)
Active treatment with functional electrical stimulation
Eligibility Criteria
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Inclusion Criteria
* Verified sleep bruxism
* More than 18 Years
* Signed ICF
Exclusion Criteria
* Pacemaker
18 Years
ALL
No
Sponsors
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Medotech A/S
INDUSTRY
Responsible Party
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Medotech A/S
Principal Investigators
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Pernille Wendelboe, MsSc (Odont)
Role: STUDY_CHAIR
Medotech A/S
Locations
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Odontologisk Institute
Aarhus, , Denmark
Countries
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Other Identifiers
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TMD-02
Identifier Type: -
Identifier Source: org_study_id
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