Treatment Sleep Bruxism With the Luco Hybrid OSA Appliance (LucoHybrid)
Primary Purpose
Sleep Bruxism, Tension Headache, Migraine Headache
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
The Luco Hybrid OSA Appliance
Sponsored by
About this trial
This is an interventional treatment trial for Sleep Bruxism
Eligibility Criteria
Inclusion Criteria:
- 18 years of age (adult)
- capable of giving informed consent
- met the AASM criteria for sleep bruxism
- had sound dentition
- did not have active obstructive sleep apnea(OSA)/upper airway resistance syndrome (UARS)
Exclusion Criteria:
- younger than 18
- incapable of informed consent
- did not meet the AASM criteria for sleep bruxism
- discovered OSA or UARS in the initial study
- did not have sound dentition (active caries, periodontal disease, inadequate number of teeth
- had obstructive sleep apnea/UARS
- did not complete the study
- completed the study but did not complete all aspects of the study
Sites / Locations
- Dr. K. Luco Dentistry Professional Corporation
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Active Comparator
Arm Label
Started
Completed
Arm Description
Intervention: Treatment with the Luco Hybrid OSA Appliance (LHOA) Group 1, fitted with LHOA Group 2: LHOA removed for 48 hours
Intervention: The LUco Hybrid OSA APpliance The subjects that actually completed the study in both groups. Group 1 n = 32, in Group 2 n=19
Outcomes
Primary Outcome Measures
Response to treatment with the Luco Hybrid OSA Appliance
Clinical examination, sleep study and visual analog scale. Clinical examination of the subject's musculature, temporomandibular joints (TMJ), and measurement of the range of mandibular movements. The home sleep study (HSS) measured the number and duration of sleep bruxism events as well as the heart rate associated with these events. The visual analog scale (VAS) recorded the patient's response regarding TMJ pain on waking and later in the day, jaw muscle pain on waking and later in the day, tooth sensitivity to temperature extremes, tension/migraine type headaches on waking and later in the day and neck/shoulder pain on waking and later in the day.
HSS scoring according to the American Academy of Sleep Medicine's "Manual for the Scoring of Sleep and Associated Events" for sleep bruxism.
Secondary Outcome Measures
Full Information
NCT ID
NCT02882880
First Posted
August 21, 2016
Last Updated
February 16, 2021
Sponsor
Luco Hybrid OSA Appliance Inc.
1. Study Identification
Unique Protocol Identification Number
NCT02882880
Brief Title
Treatment Sleep Bruxism With the Luco Hybrid OSA Appliance
Acronym
LucoHybrid
Official Title
The Treatment of Sleep Bruxism With the Luco Hybrid OSA Appliance
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
July 2015 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
July 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Luco Hybrid OSA Appliance Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To determine the effectiveness of the Luco Hybrid OSA Appliance in the treatment of sleep bruxism and to aid in the treatment of associated tension/migraine type headaches in adults.
Detailed Description
51 subjects were selected and separated into two groups: those new to the treatment (Group 1)and those who had been in treatment for more than 1 year (Group 2). There were 32 participants in group 1 and 19 in group 2. mean age for Group 1 was 41.7 and Group 2 was 50.5. The age range for Group 1 was 21 to 66 and in Group 2 34 to 73.
Group 1 subjects were fitted with a Luco hybrid OSA appliance (LHOA). They were followed over a 14 day period with adjustments made to the device as required. The second study [milestone] was completed at that time.
Group 2 subjects, who had previously been in treatment with the device for and mean of 4.1 years, had an initial study with the device and a second study following 48 hours without the device.
Both groups were studied again at 60 days and results compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Bruxism, Tension Headache, Migraine Headache
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Non-Randomized
Enrollment
51 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Started
Arm Type
Other
Arm Description
Intervention: Treatment with the Luco Hybrid OSA Appliance (LHOA) Group 1, fitted with LHOA Group 2: LHOA removed for 48 hours
Arm Title
Completed
Arm Type
Active Comparator
Arm Description
Intervention: The LUco Hybrid OSA APpliance The subjects that actually completed the study in both groups. Group 1 n = 32, in Group 2 n=19
Intervention Type
Device
Intervention Name(s)
The Luco Hybrid OSA Appliance
Other Intervention Name(s)
Mandibular advancement appliance
Intervention Description
Group 1, initial treatment with the device, reassessed at 14 and 60 days, Group 2, removal of the treatment for 48 hours, to determine if relapse occurs, retested at 60 days with the device (recovery from intervention).
Primary Outcome Measure Information:
Title
Response to treatment with the Luco Hybrid OSA Appliance
Description
Clinical examination, sleep study and visual analog scale. Clinical examination of the subject's musculature, temporomandibular joints (TMJ), and measurement of the range of mandibular movements. The home sleep study (HSS) measured the number and duration of sleep bruxism events as well as the heart rate associated with these events. The visual analog scale (VAS) recorded the patient's response regarding TMJ pain on waking and later in the day, jaw muscle pain on waking and later in the day, tooth sensitivity to temperature extremes, tension/migraine type headaches on waking and later in the day and neck/shoulder pain on waking and later in the day.
HSS scoring according to the American Academy of Sleep Medicine's "Manual for the Scoring of Sleep and Associated Events" for sleep bruxism.
Time Frame
60 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18 years of age (adult)
capable of giving informed consent
met the AASM criteria for sleep bruxism
had sound dentition
did not have active obstructive sleep apnea(OSA)/upper airway resistance syndrome (UARS)
Exclusion Criteria:
younger than 18
incapable of informed consent
did not meet the AASM criteria for sleep bruxism
discovered OSA or UARS in the initial study
did not have sound dentition (active caries, periodontal disease, inadequate number of teeth
had obstructive sleep apnea/UARS
did not complete the study
completed the study but did not complete all aspects of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ken J Luco, DDS, BSc
Organizational Affiliation
Luco Hybrid OSA Appliance Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr. K. Luco Dentistry Professional Corporation
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 0C3
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
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Available IPD and Supporting Information:
Available IPD/Information Type
Informed Consent Form
Available IPD/Information URL
http://lucohybridosa.com/wp-content/uploads/2016/08/INFORMED-CONSENT.pdf
Available IPD/Information Identifier
Informed Consent
Available IPD/Information Type
Clinical Study Report
Available IPD/Information URL
http://lucohybridosa.com/wp-content/uploads/2016/08/CLINICAL-STUDY-REPORT.pdf
Available IPD/Information Identifier
Study Report
Learn more about this trial
Treatment Sleep Bruxism With the Luco Hybrid OSA Appliance
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