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Clinical Study of Customized Adjustable Oral in Treatment of Patients With Obstructive Sleep Apnea Syndrome

Primary Purpose

Obstructive Sleep Apnea Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Adjustable Oral Appliance
Sponsored by
Affiliated Hospital to Academy of Military Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnea Syndrome focused on measuring Orthodontic Appliances, Cone-Beam Computed Tomography

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Apnea-hypopnea index(AHI)between 5/h and 45/h
  • Aged between 18 and 50 years old
  • Intolerance to continuous positive airway pressure or surgery
  • Body Mass Index(BMI) <35kg/m
  • Those who are competent to give written informed consent
  • Have adequate tooth support to retain the oral appliance

Exclusion Criteria:

  • Previous or current treatment for OSAS
  • Presence of respiratory/sleep disorders other than obstructive sleep apnea
  • Medication usage that could influence respiration or sleep
  • Concurrent unstable cardiovascular disease,neurological or mental disorders
  • Active periodontal endodontic disease or open bite
  • Temporomandibular joint disorders
  • Loss of posterior dental support to undermine the retention of oral appliance
  • Pregnancy

Sites / Locations

  • Chiese PLA 307 hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

patients with OSAS in different degrees

Arm Description

OSAS patients will be treated with an adjustable oral appliance and evaluated with cone-beam computed tomography and polysomnography.

Outcomes

Primary Outcome Measures

change in apnea hypopnea index(AHI)
the change from apneas hypopneas per hour of sleep registration of the subjects fitted with oral appliance at 3,6 and 10 months

Secondary Outcome Measures

change in apnea index(AI)
the change from apneas per hour of sleep registration of the subjects fitted with oral appliance at 3,6 and 10 months
change in lowest blood oxygen saturation
the change from the ratio of the content of oxyhaemoglobin to the content of oxygenic hemoglobin in the blood of the subjects at 3,6 and 10 months
change in minimal volume/transverse diameter/sagittal diameter/cross-sectional area of the velopharyngeal segment of the subjects
the change from velopharyngeal segment of upper airway is the region between two planes pass separately through the posterior nasal spine point (PNS) and the tip of soft palate point(U),which are parallel to frankfort horizontal plane(FH) after 3,6 and 10 months
change in minimal volume/transverse diameter/sagittal diameter/cross-sectional area of the oropharyngeal segment of upper airway
the change from oropharyngeal segment of upper airway is the region between two planes pass separately through the highest point of epiglottis(EP) and the tip of soft palate point(U),which are parallel to frankfort horizontal plane(FH) at 3,6 and 10 months

Full Information

First Posted
September 24, 2018
Last Updated
November 1, 2018
Sponsor
Affiliated Hospital to Academy of Military Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT03729895
Brief Title
Clinical Study of Customized Adjustable Oral in Treatment of Patients With Obstructive Sleep Apnea Syndrome
Official Title
Clinical Effect and Upper Airway Changes of Customized Adjustable Oral Appliance in the Treatment of Patients With Obstructive Sleep Apnea Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 2018 (Anticipated)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
October 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Affiliated Hospital to Academy of Military Medical Sciences

4. Oversight

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

5. Study Description

Brief Summary
The oral appliances (OAs) are considered to be an effective treatment modality for snoring and various forms of obstructive sleep apnea syndrome (OSAS). They facilitate the displacement of the mandible anteriorly and widen the upper airway during sleep. Lateral cephalometry has been used for the two-dimensional evaluation of upper airway form with several limits.The purpose of present study is to investigate an accurate three-dimensional (3D) volume analyses with cone beam computed tomography (CBCT) scans to confirm the effects of OAs on the upper airway in patients with OSAS.The investigators aim to enroll twenty-four patients with mild,moderate or severe OSAS, intolerant to continuous positive air pressure therapy and rejection a surgical approach,who will be treated with adjustable customized OAs and evaluated with CBCT and polysomnography. Upper airway form was examined and the volume was measured in two different areas. Specific planes have been considered to match the data and calculate the benefit obtained with therapy.
Detailed Description
Obstructive sleep apnea syndrome (OSAS) represents the most common nocturnal respiratory disease characterized by repetitive episodes of partial or complete upper airway collapse or narrowing during sleep,associated with phasic oxygen desaturation.Failure to recognize this condition could lead to an increased risk of cardiovascular diseases, daytime sleepiness, road accidents, a reduced cognitive capacity, with a decline of the quality of life.According to the American Association of Sleep Medicine,the diagnostic standard of the OSAS is the polysomnographic exam, which allows to assess the gravity of OSAS in relation to the Apnea Hypopnea Index (AHI) within an hour:slight (AHI<5), moderate (5<AHI<30) and severe (AHI>30). Epidemiological investigations has shown that the prevalence rate of OSAS is 2-4% of the total population,whereas the percentage of undiagnosed OSAS remains very high with progression to dangerous complications. OSAS treatment modalities include proper body position, slimming,continuous positive air pressure(CPAP),surgical procedures and oral appliances use. OA are dental devices that improve OSAS by producing a structural change of the upper airways, in order to mechanically increase the pharyngeal diameters, keep the tongue from falling backwards and to stiffen the pharyngeal muscles longitudinally.Recently, OAs is growing more popular due to its superiority in the treatment of the OSAS.It offers a non-invasive form of treatment but also achieve a good therapeutic effect. Traditionally, the effects of functional appliances are evaluated using two-dimensional (2D) radiographs, but the reproducibility of 2D is complex, and overlapping images are difficult to assess. Cone-beam computed tomography (CBCT) provides more accurate and reproducible imaging for assessing all craniofacial skeletal structures. The objective of this study was to evaluate, in a 6-months follow-up study, the effect of costumed adjustable oral appliance in OSAS patients both through the comparison of the polysomnographic analysis, and also through the volumetric measurements of the pharyngeal airway by using the cone beam computed tomography. Twenty-four patients,aged 18 to 50 years,in whom the diagnosis of OSAS was made following polysomnography in a sleep laboratory will be enrolled between September 2018 and November 2018.All patients will also undergo a systematic dental examination by a dentist, which put an indication to the use of OA, based also on the craniofacial features assessment. The Epworth Sleepiness Scale (ESS) will be used to evaluate daytime sleepiness. They then will be fitted with a costumed adjustable oral appliance. The appliances are taken with a mandibular advancement of 2-3 mm and vertical rise of 4-5 mm, that is, the vertical position set at the minimum occlusal elevation to allow mandibular advancement and to avoid backward rotation. The participants were asked to wear the test appliance for 7 nights, and in case of compliance,application it every night at least for 6 months. The selected patients will be record their usage of the appliance and any adverse effects in a treatment journal. The research focus on the following outcomes: sleep apnea and the the volumetric changes of the upper airway. All patients were radiographically evaluated with a specific diagnostic examination: the cone beam computed tomography scan. For each patient, 3 CBCT scans were performed positioning his head in a neutral way and were performed without swallowing or respiratory movements during inspiration at rest: the first one before the therapy, the second after 3 months and the second after 6 months. Data obtained through CBCT scans have been exported in DICOM format and analyzed with a specific software (MIMICS-Materialise Interactive Medical Image Control System, Leuven, Belgium).The pharyngeal area around the velopharynx and oropharynx has been considered in which the origin of apneas is mainly found.Three planes have been built, an upper, a middle, and lower one, all perpendicular to the median sagittal plane of symmetry to obtain 2 areas, a superior and an inferior one.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea Syndrome
Keywords
Orthodontic Appliances, Cone-Beam Computed Tomography

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Twenty-four patients diagnosed with OSAS in different degrees,who cannot tolerate continuous positive air pressure use and reject a surgical approach, were treated with adjustable customized oral appliances and evaluated with cone-beam computed tomography and polysomnography.
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
patients with OSAS in different degrees
Arm Type
Experimental
Arm Description
OSAS patients will be treated with an adjustable oral appliance and evaluated with cone-beam computed tomography and polysomnography.
Intervention Type
Device
Intervention Name(s)
Adjustable Oral Appliance
Intervention Description
Adjustable Oral Appliance consist of plastic maxillary occlusal splint,mandible occlusal splint and adjustable connecting rod.It could offer a non-invasive form of treatment but also achieve a good therapeutic effect
Primary Outcome Measure Information:
Title
change in apnea hypopnea index(AHI)
Description
the change from apneas hypopneas per hour of sleep registration of the subjects fitted with oral appliance at 3,6 and 10 months
Time Frame
3,6 and 10 months
Secondary Outcome Measure Information:
Title
change in apnea index(AI)
Description
the change from apneas per hour of sleep registration of the subjects fitted with oral appliance at 3,6 and 10 months
Time Frame
3,6 and 10 months
Title
change in lowest blood oxygen saturation
Description
the change from the ratio of the content of oxyhaemoglobin to the content of oxygenic hemoglobin in the blood of the subjects at 3,6 and 10 months
Time Frame
3,6 and 10 months
Title
change in minimal volume/transverse diameter/sagittal diameter/cross-sectional area of the velopharyngeal segment of the subjects
Description
the change from velopharyngeal segment of upper airway is the region between two planes pass separately through the posterior nasal spine point (PNS) and the tip of soft palate point(U),which are parallel to frankfort horizontal plane(FH) after 3,6 and 10 months
Time Frame
3,6 and 10 months
Title
change in minimal volume/transverse diameter/sagittal diameter/cross-sectional area of the oropharyngeal segment of upper airway
Description
the change from oropharyngeal segment of upper airway is the region between two planes pass separately through the highest point of epiglottis(EP) and the tip of soft palate point(U),which are parallel to frankfort horizontal plane(FH) at 3,6 and 10 months
Time Frame
3,6 and 10 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Apnea-hypopnea index(AHI)between 5/h and 45/h Aged between 18 and 50 years old Intolerance to continuous positive airway pressure or surgery Body Mass Index(BMI) <35kg/m Those who are competent to give written informed consent Have adequate tooth support to retain the oral appliance Exclusion Criteria: Previous or current treatment for OSAS Presence of respiratory/sleep disorders other than obstructive sleep apnea Medication usage that could influence respiration or sleep Concurrent unstable cardiovascular disease,neurological or mental disorders Active periodontal endodontic disease or open bite Temporomandibular joint disorders Loss of posterior dental support to undermine the retention of oral appliance Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
biao Guo, master
Phone
0086-010-66947095
Email
418406096@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
rongjian Lu, doctor
Organizational Affiliation
Chinese PLA 307 Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Chiese PLA 307 hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100071
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
rongjian Lu, doctor
Phone
0086-010-66947334
Email
13426301158@163.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Clinical Study of Customized Adjustable Oral in Treatment of Patients With Obstructive Sleep Apnea Syndrome

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