A Clinical Trial of the Optimal Treatment Period and Long-term Efficacy of Functional Electrical Stimulation (FES) on Sleep Bruxism

Medotech A/S23 enrolled

Overview

To investigate the effect of the treatment with Grindcare® on the parafunction of the muscles- and jaw activity (Bruxism) during sleep.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Temporomandibular Disorder Headache

Interventions

Grindcare® (Biofeedback)DEVICE

Active treatment with functional electrical stimulation

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * RDC-TMD diagnosis * Verified sleep bruxism * More than 18 Years * Signed ICF Exclusion Criteria: * Contraindication of concomitant medication and diseases judged by investigator * Pacemaker

Locations (1)

Odontologisk Institute

Aarhus, Denmark

Outcomes

Primary Outcomes

Reduction of number of grinds per hour per night

Time frame: 7 weeks

Data from ClinicalTrials.gov

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