Control of parafunction with bite plane therapy

Not Applicable

Completed

• Conditions: TMD, MPD, Sleep Stages; Not Applicable

• Registration Number: ISRCTN26019919
• Lead Sponsor: Ontario Thoracic Society Block Term Grant

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2001-02-01
• Study Start: 2017-11-02
• Last Update Posted: 29 April 2019

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

1. Permanent dentitions with no more than 1 tooth missing per quadrant (excluding wisdom teeth)
2. No implants or partial dentures
3. Not undergoing current treatment for TMD/MPD
3. Females aged 20-57

Exclusion Criteria

1. Male
2. Children and seniors
3. Multiple missing teeth in each quadrant
4. Dental implants
5. Partial dentures
6. Active treatment for TAD/MPD

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> 1. TMD symptoms are measured using the TMJ scale at baseline and study end<br> 2. Bruxism is measured using the polysomnograph at baseline and study end<br> 3. Daytime sleepiness is measured using Epworth Sleepiness Scale at baseline and study end<br> 4. Pain symptoms with treatment is measured using the McGill pain questionnaire at baseline and study end<br> 5. Patient symptoms are measured using the Helkimo Index at baseline and study end<br>

Secondary Outcome Measures

Name	Time	Method
There are no secondary outcome measures.