Differences in Predicted Therapeutic Outcome of Oral Appliance Determined by RCMP in Quebec Versus Shenyang Patients With OSA.

Sponsor
First Hospital of China Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03231254
Collaborator
Laval University (Other)
100
2
3.9
50
12.7

Study Details

Study Description

Brief Summary

Study Objective: To explore the differences in predicted therapeutic outcome of OA and optimal protrusion position determined by Remotely Controlled Mandibular Positioner (RCMP) with overnight PSG in Quebec versus Shenyang patients with OSA.

Design: A prospective, inter-ethnic pilot study. Setting: Two Standard sleep disorder clinical care in Quebec (Canada) and Shenyang (China), with oral appliance titration tests performed in sleep laboratory.

Participants: Consecutive specific OSA patients, who are potential candidates for treatment of OSA with an oral appliance (n=100, 50 Canadian, 50 Chinese), will be recruited from a sleep center or respirologists, psychiatrists, otolaryngologist and dentists practicing with broad inclusion criteria (age: 20-75 years, AHI:15-50/h; BMI<40 kg/m2).

Interventions: A mandibular protrusive titration study in the PSG lab using a RCMP not only predicts the eventual therapeutic outcome but also prospectively determines Optimal Protrusive Position (OPP) for participants predicted to be therapeutically successful with OA therapy. One goal of this study is to identify OA favorable candidates by physicians using prospectively and explicitly designed criteria. Analyses of the predicted therapeutic outcome of OA and OPP between the two ethnic populations (patients in Quebec and Shenyang) will be processed after matching for OSA severity.

Condition or Disease Intervention/Treatment Phase
  • Device: Remotely Controlled Mandibular Positioner (RCMP)

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Differences in Predicted Therapeutic Outcome of Oral Appliance and Optimal Protrusion Position Determined by Remotely Controlled Mandibular Positioner (RCMP) With Overnight PSG in Quebec Versus Shenyang Patients With OSA
Actual Study Start Date :
Jul 1, 2017
Anticipated Primary Completion Date :
Oct 20, 2017
Anticipated Study Completion Date :
Oct 29, 2017

Arms and Interventions

Arm Intervention/Treatment
Chinese patients with OSA

Device: Remotely Controlled Mandibular Positioner (RCMP)
RCMP device can accurately identify patients who are likely to be successful OA candidates. With a temporary dental appliance connected to a RCMP, the mandible could be progressively, mildly and precisely protruded in only anterior-posterior dimension, under the monitor of PSG, without disturbing sleep, until obstructive apneas and hypopneas were eliminated, particularly in REM sleep while supine. Besides, RCMP device can also determine the optimal therapeutic level of mandibular protrusion during sleep.

Canada patients with OSA

Device: Remotely Controlled Mandibular Positioner (RCMP)
RCMP device can accurately identify patients who are likely to be successful OA candidates. With a temporary dental appliance connected to a RCMP, the mandible could be progressively, mildly and precisely protruded in only anterior-posterior dimension, under the monitor of PSG, without disturbing sleep, until obstructive apneas and hypopneas were eliminated, particularly in REM sleep while supine. Besides, RCMP device can also determine the optimal therapeutic level of mandibular protrusion during sleep.

Outcome Measures

Primary Outcome Measures

  1. The differences of predicted therapeutic outcome of OA between two groups. [2017.7-2017.11]

    To identify and compare the number of OA favorable candidates by physicians using prospectively and explicitly designed criteria in both groups.

Secondary Outcome Measures

  1. The differences of optimal protrusion position determined by Remotely Controlled Mandibular Positioner (RCMP) with overnight PSG in Quebec versus Shenyang patients with OSA. [2017.7-2017.11]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Recent diagnosis of OSAS (AHI>15/h) announced by a sleep recording; mean oxygen saturation >90%; mandibular range of motion >5 mm; adequate dentition: ≥10 upper and 10 lower teeth.
Exclusion Criteria:
  • (1). Body mass index 40 kg/m2 or greater; (2).Inability to tolerate overnight polysomnography in sleep lab; (3).>50% of observed sleep apneas being central; (4). Other sleep disorders such as insomnia, narcolepsy, chronic sleep deficiency, periodic limb movement disorder or restless legs syndrome; (5). Those with severe pharyngeal obstruction on physical exam (pharyngeal grade more than II); (6).severe nasal obstruction.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Frederic Series Quebec City Quebec Canada G1V 4G5
2 Wenyang Li Shenyang Liaoning China 110001

Sponsors and Collaborators

  • First Hospital of China Medical University
  • Laval University

Investigators

  • Principal Investigator: Wei Wang, PhD, First Hospital of China Medical University
  • Study Director: Frederic Series, master, Pneumologue Institut Universitaire de Cardiologie et de Pneumologie de Québec

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wenyang Li, Medical doctor, First Hospital of China Medical University
ClinicalTrials.gov Identifier:
NCT03231254
Other Study ID Numbers:
  • AF-SOP-07-1.0-01
First Posted:
Jul 27, 2017
Last Update Posted:
Jul 27, 2017
Last Verified:
Jul 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No

Study Results

No Results Posted as of Jul 27, 2017