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Pressure Algometry Evaluation of Two Occlusal Splint Designs in Bruxism Management - RCT

Primary Purpose

Bruxism, Sleep Disorder

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Two different occlusal splints
Sponsored by
Pomeranian Medical University Szczecin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Bruxism focused on measuring bruxism, algometer, pressure pain threshold, occlusal, splint, grinding, clenching

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • I. Nocturnal Bruxism according to International Classification of Sleep Disorders, Second Edition (ICSD-2).

A. The patient reports or is aware of tooth-grinding sounds or tooth clenching during sleep.

B. One or more of the following is present: a. Abnormal wear of teeth b. Jaw muscle discomfort, fatigue, or pain and jaw lock upon awakening. c. Masseter muscle hypertrophy upon voluntary forceful clenching.

C. The jaw muscle activity is not better explained by another current sleep disorder, medical or neurological disorder, medication use, or substance use disorder.

II. Additional questionnaire for detecting bruxers:

Has anyone heard you grinding your teeth at night? Is your jaw ever fatigued or sore in the morning? Are your teeth or gums ever sore on awakening in the morning? Do you ever experience temporal headaches on awakening in the morning? Are you aware of grinding your teeth during the day? Are you ever aware of clenching your teeth during the day Can you imitate a sound of grinding using your teeth.

Exclusion Criteria:

  • unrestored tooth losses
  • patients wearing removable dentures of any kind
  • psychiatric conditions undermining/preventing occlusal splint usage

Sites / Locations

  • Chair and Depratment of Dental ProstheticsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Occlusal appliance by Okeson with canone guidance

Bimaxillary splint without canine guidance

Arm Description

Occlusal appliance will be used while sleeping for 30 days.

Bimaxillary splint will be used while sleeping for 30 days.

Outcomes

Primary Outcome Measures

Pressure pain threshold in designated points
Evaluation of difference between algometer readings before and after 30 days of splint usage - FPX25 algometer (Wagner instruments, US) will be used

Secondary Outcome Measures

Full Information

First Posted
January 26, 2021
Last Updated
June 16, 2021
Sponsor
Pomeranian Medical University Szczecin
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1. Study Identification

Unique Protocol Identification Number
NCT04733573
Brief Title
Pressure Algometry Evaluation of Two Occlusal Splint Designs in Bruxism Management - RCT
Official Title
Pressure Algometry Evaluation of Two Occlusal Splint Designs in Bruxism Management - Randomized, Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
June 16, 2021 (Actual)
Study Completion Date
June 30, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pomeranian Medical University Szczecin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
During the study, designated pressure points before and after one month of splint usage will be evaluated as possible indicators of two different splints efficacy.. Two study groups will be formed. The study will be conducted on patients reporting to the Dental Prosthetics Outpatient Clinic of PUM in Szczecin, Poland. Patients aged 18-65 years with probable bruxism, yet requiring splint therapy will be included in the study.
Detailed Description
During the study, designated pressure points before and after one month of splint usage will be evaluated as possible indicators of two different splints efficacy.. Two study groups will be formed. The study will be conducted on patients reporting to the Dental Prosthetics Outpatient Clinic of PUM in Szczecin, Poland. Patients aged 18-65 years with probable bruxism, yet requiring splint therapy will be included in the study. Probable bruxism will be diagnosed on the basis of the patient's history and examination as follows. Inclusion criteria: I. Nocturnal Bruxism according to International Classification of Sleep Disorders, Second Edition (ICSD-2). A. The patient reports or is aware of tooth-grinding sounds or tooth clenching during sleep. B. One or more of the following is present: a. Abnormal wear of teeth b. Jaw muscle discomfort, fatigue, or pain and jaw lock upon awakening. c. Masseter muscle hypertrophy upon voluntary forceful clenching. C. The jaw muscle activity is not better explained by another current sleep disorder, medical or neurological disorder, medication use, or substance use disorder. II. Additional questionnaire for detecting bruxers: Has anyone heard you grinding your teeth at night? Is your jaw ever fatigued or sore in the morning? Are your teeth or gums ever sore on awakening in the morning? Do you ever experience temporal headaches on awakening in the morning? Are you aware of grinding your teeth during the day? Are you ever aware of clenching your teeth during the day Can you imitate a sound of grinding using your teeth. III. Eligible patients will be randomly assigned into two groups. Sealed, opaque envelopes will be used for randomization. The first group will be treated with a stabilization appliance described by Okeson. The second group will undergo therapy with a two-jaw splint with an arch. Patients will be informed about how to use and maintain hygiene of the splint. It will be recommended to use a splint only while sleeping. IV. Pressure pain threshold test (PPT) will be carried out at the Department of Prosthodontics of the Pomeranian Medical University, Szczecin, Poland using the Wagner Paintest FPX 25 algometer. Points within the following muscles will be examined: masseter muscles, anterior, middle and posterior abdomens of the temporal muscles, a point at the height of the TMJ larger exterior convexity, the sternocleidomastoid muscles and the preauriculare point, bilaterally two measurements at each visit. The test will be performed at the first visit and after 30 days of therapy. The algometer comes with a 1 cm2 rubber tip, which measures the pressure in kg / s while pressing on the tested surface. Both test results will be used as a pre- and post- treatment evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bruxism, Sleep Disorder
Keywords
bruxism, algometer, pressure pain threshold, occlusal, splint, grinding, clenching

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Occlusal appliance by Okeson with canone guidance
Arm Type
Active Comparator
Arm Description
Occlusal appliance will be used while sleeping for 30 days.
Arm Title
Bimaxillary splint without canine guidance
Arm Type
Active Comparator
Arm Description
Bimaxillary splint will be used while sleeping for 30 days.
Intervention Type
Device
Intervention Name(s)
Two different occlusal splints
Intervention Description
Two different occlusal splints will be used for bruxism management, PPT would be evaluated twice - before and after 30 days of splint therapy using pressure algometer (FPX25, Wagner Instruments, US)
Primary Outcome Measure Information:
Title
Pressure pain threshold in designated points
Description
Evaluation of difference between algometer readings before and after 30 days of splint usage - FPX25 algometer (Wagner instruments, US) will be used
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: I. Nocturnal Bruxism according to International Classification of Sleep Disorders, Second Edition (ICSD-2). A. The patient reports or is aware of tooth-grinding sounds or tooth clenching during sleep. B. One or more of the following is present: a. Abnormal wear of teeth b. Jaw muscle discomfort, fatigue, or pain and jaw lock upon awakening. c. Masseter muscle hypertrophy upon voluntary forceful clenching. C. The jaw muscle activity is not better explained by another current sleep disorder, medical or neurological disorder, medication use, or substance use disorder. II. Additional questionnaire for detecting bruxers: Has anyone heard you grinding your teeth at night? Is your jaw ever fatigued or sore in the morning? Are your teeth or gums ever sore on awakening in the morning? Do you ever experience temporal headaches on awakening in the morning? Are you aware of grinding your teeth during the day? Are you ever aware of clenching your teeth during the day Can you imitate a sound of grinding using your teeth. Exclusion Criteria: unrestored tooth losses patients wearing removable dentures of any kind psychiatric conditions undermining/preventing occlusal splint usage
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bartosz Dalewski, DMD, PhD
Phone
0048 914661717
Email
bartosz.dalewski@pum.edu.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Kamila Szczuchniak, DMD
Phone
0048 914661717
Email
kamila.szczuchniak@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agata Kamińska, DMD
Organizational Affiliation
Pomeranian Medical Universiy in Szczecin, Poland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chair and Depratment of Dental Prosthetics
City
Szczecin
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bartosz Dalewski, DMD, PhD
First Name & Middle Initial & Last Name & Degree
Kamila Szczuchniak, DMD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34071832
Citation
Dalewski B, Kaminska A, Kiczmer P, Wegrzyn K, Palka L, Janda K, Sobolewska E. Pressure Algometry Evaluation of Two Occlusal Splint Designs in Bruxism Management-Randomized, Controlled Clinical Trial. J Clin Med. 2021 May 27;10(11):2342. doi: 10.3390/jcm10112342.
Results Reference
background
Links:
URL
https://pubmed.ncbi.nlm.nih.gov/34071832/
Description
https://www.mdpi.com/2077-0383/10/11/2342

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Pressure Algometry Evaluation of Two Occlusal Splint Designs in Bruxism Management - RCT

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