Trials / Unknown
UnknownNCT03180671
Anterior Deprogrammers for Reducing Pain and Masticatory Muscles Tension
The Effectiveness of Anterior Deprogrammers as a Tool for Reducing Pain and Masticatory Muscles Tension
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Lukasz Adamczyk · Academic / Other
- Sex
- All
- Age
- 20 Years – 30 Years
- Healthy volunteers
- Not accepted
Summary
The study will be conducted in four groups of 20 patients in age of 20-30 years with complete dentition or single tooth loss in lateral regions, with masticatory muscle pain in the history or during examination and overuse and/or chronic tensing of the masticatory muscles. Patients will be randomly assigned to the groups. Each person will be measured twice before and after use of selected anterior deprogrammer. The following assessment tools will be applied: * surface electromyography of masseter and temporal muscles, * intraoral pin-supported registration to draw a gothic arch. Measurements will be made before and after intervention to assess the effect of anterior deprogrammer application on the tone of the selected masticatory muscles and condyles position in mandibular fossa. The first group (control) will be counsel with an explanation of the pathomechanism of masticatory muscles pain and preventive principles. In the second group, the Sliding Guide will be used for a period of 12-15 minutes, in the third Dawson B-Splint for 7 days, and in the fourth Kois deprogrammer for 14 days. Devices in group 3 and 4 will be used by patients for 24 hours a day, with breaks for oral hygiene procedures and eating/drinking. The aim of the study is to evaluate the effectiveness of selected anterior deprogrammers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Deprogramer Sliding Guide | Use of the intraoral device. |
| DEVICE | Deprogrammer Dawson B-Splint | Use of the intraoral device. |
| DEVICE | Deprogrammer Kois | Use of the intraoral device. |
Timeline
- Start date
- 2017-04-01
- Primary completion
- 2019-01-01
- Completion
- 2019-05-01
- First posted
- 2017-06-08
- Last updated
- 2017-06-08
Locations
1 site across 1 country: Poland
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03180671. Inclusion in this directory is not an endorsement.