Clinical Trials Logo

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03435731
Other study ID # H18-00175
Secondary ID FCRC1801
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date March 8, 2018
Est. completion date December 2018

Study information

Verified date April 2018
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Continuous positive airway pressure (CPAP) is considered the gold standard therapy for obstructive sleep apnea (OSA). However, CPAP users sometimes experience pressure-related discomfort. It is thought that lower CPAP pressure may increase comfort and lead to greater treatment adherence.

Mandibular advancement splint (MAS) therapy has been shown to be the preferred OSA treatment option among patients. However, MAS therapy is only partially effective in some OSA patients, especially in severe cases.

It is thought that a combination of MAS and PAP therapy may benefit patients in which MAS alone is only partially effective. Using MAS and PAP at the same time is called "Dual Therapy". Dual Therapy may allow a lower CPAP pressure to be applied, which may increase patient comfort and therefore increase treatment adherence and overall effectiveness.

This study will evaluate the effectiveness of 1 month of Dual Therapy in 30 OSA patients.


Description:

This is a prospective clinical trial assessing the effect of 1-month of dual therapy on patients with varying baseline OSA severity (mild to severe) who have been previously fully titrated to both PAP and MAS.

This study will be conducted at 2 research centers; the Faculty of Dentistry, University of British Columbia (UBC), Vancouver and at the Faculty of Dentistry, Université de Montréal (UdM), Montréal.

The research team will access participants' records to confirm eligibility for dual therapy. The clinical research coordinator will contact eligible patients via phone to ask if they are interested in taking part in the study. Eligible patients will also be asked if they are interested in taking part in the study during routine clinic visits. Where possible, patients will not be approached by their primary caregiver regarding participation in this study, to ensure patients do not feel pressurized into participating. Choosing not to take part in the study will not affect the participants' quality of care. If a patient is interested in taking part in the study they will be invited to review and sign the informed consent form.

Consenting participants will be asked to use both MAS and PAP (dual therapy) together for a period of 1 month. During the first week of the dual therapy, PAP pressure will be adjusted automatically for a 1-week period, after which the pressure will be set remotely by the Respiratory Therapist at the 90th percentile.

With permission, the research team will access the Sleep Apnea Dental Clinic records to collect data relating to previous treatment with MAS and PAP monotherapies. Data collected includes: PAP pressure, treatment adherence, subjective treatment assessment, Epworth Sleepiness Scale (ESS) and Functional Outcomes of Sleep Questionnaires (FOSQ), weight, blood pressure and oximetry data.

At the end of the 1-month, a subjective and objective assessment will be conducted. Subjective data will be collected using a short questionnaire that will be completed by the participants pertaining to their experience with the dual therapy in addition to completing a short term medical/treatment update form. Participants' weight and blood pressure will also be reassessed. Objective adherence will be analyzed via data obtained from the PAP modem and from DentiTrac® smart chips embedded in the MAS. OSA-related quality of life will be reassessed using ESS and FOSQ questionnaires.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 30
Est. completion date December 2018
Est. primary completion date October 2018
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

- Age 19-80 years old who are able to freely provide informed consent;

- Prior participation in the CHOICE study;

- Have been optimally titrated to PAP and MAS therapy;

- Have both PAP and MAS appliances at home and ready for use;

- Body mass index (BMI) of 35 or less;

- = 8 teeth per arch to support treatment with MAS;

- Have an objective of diagnosis of OSA based on the following criteria:

- - an Apnea-Hypopnea Index (AHI) within the range 10 = AHI = 70 documented with polysomnography in the last 2 years; ***OR***

- - a Respiratory Disturbance Index (RDI) within the range 20 = RDI = 70 documented with level III portable sleep test; ***OR***

- - an Oxygen Desaturation Index (ODI) = 10;

- Sleep investigations confirming the object diagnosis of OSA have been performed within the past 4 years

Exclusion Criteria:

- Use of a full face mask as the PAP interface;

- Extensive periodontal disease with significant tooth mobility;

- Inability to protrude jaw;

- Insufficient vertical opening to accommodate treatment with MAS;

- Uncontrolled congestive heart failure (defined as a prior clinical diagnosis, an ejection cut-off of 40% or clinical sign in the opinion of a primary care physician or cardiologist) that makes it unsafe in the opinion of the investigators for the subject to participate in the trial;

- Coronary artery disease unless stable for at least 6 months and considered by the investigators to have a stable disease;

- Any history of angina, myocardial infarction or stroke;

- Any history of major depressive disorder along with current moderate-severe disease;

- Active cancer management (unless in remission for more than 1 year);

- Known renal failure (with need for dialysis);

- History of a near miss or prior automobile accident due to sleepiness within the past 12 months;

- At nighttime, 30% of the night is at = 90% oxygen saturation levels.

Study Design


Intervention

Combination Product:
Dual Therapy
Concomitant use of Continuous Positive Airway Pressure (CPAP) and Mandibular Advancement Splint (MAS) therapeutic devices.

Locations

Country Name City State
Canada Université de Montréal Montréal Quebec
Canada University of British Columbia Vancouver British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Université de Montréal

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in CPAP Pressure Optimal CPAP Pressure determined by the Respiratory Therapist (cmH2O) Baseline (from previous treatment with CPAP) and 1 month after commencing Dual Therapy treatment.
Primary Comfort A subjective assessment of the Dual Therapy treatment, reported via a questionnaire. Baseline (from previous treatment) and 1 month after commencing Dual Therapy treatment.
Primary Treatment Adherence (hrs/night) Adherence measured in hours per night. The duration of Dual Therapy treatment (1 month).
Primary Treatment Adherence (% nights) Adherence measured in percentage of nights of use. The duration of Dual Therapy treatment (1 month).
Secondary Daytime Sleepiness Evaluation of OSA specific fatigue using Epworth Sleepiness Scale (ESS) questionnaire. ESS measures daytime sleepiness via 8 questions that ask about daytime sleepiness during common everyday conditions. The potential range of scores for any questions is from 0 to 3. Higher values represent worse outcomes. Their are no subscales for ESS. The answers to the questions are all summed up. Total score ranges between 0 and 24. A score above 10 indicates daytime sleepiness with higher scores indicating more sleepiness. Baseline (from previous treatment) and 1 month after commencing Dual Therapy treatment.
Secondary Quality of Life using Functional Outcomes of Sleep Questionnaire (FOSQ-10) FOSQ-10 measures functional status and difficulty in performing everyday activities via 10 questions. The range of scores for any question is from 1 to 4. There is also a 0 score option for participants who do not engage in a particular activity for other reasons, in which case the question will be excluded. There are 5 subscales that measure: general productivity, activity level, vigilance, social outcomes, and intimacy and sexual relationships. To obtain the total score, a mean-weighted item score is computed for those subscales with more than one item. To calculate a mean-weighted item score calculate the mean of the answered items with responses > 1 for each subscale. The total score is then derived by calculating the mean of the subscale scores and multiplying that mean by five. Total score ranges between 5 and 20. Higher scores indicate better functional status. Baseline (from previous treatment) and 1 month after commencing Dual Therapy treatment.
Secondary Efficacy - Oxygen Desaturation Index The number of times per hour of sleep that the blood's oxygen level drop below 97% oxygen saturation. Baseline (from previous treatment) and 1 month after commencing Dual Therapy treatment.
Secondary Efficacy - Time below 90% Saturation Percentage of time during sleep that the patient's blood oxygen levels fall below 90% saturation. Baseline (from previous treatment) and 1 month after commencing Dual Therapy treatment.
Secondary Efficacy - Minimum Saturation The lowest percentage saturation of the patient's blood oxygen levels during sleep. Baseline (from previous treatment) and 1 month after commencing Dual Therapy treatment.
See also
  Status Clinical Trial Phase
Recruiting NCT05857384 - Bioavailability, Bioequivalence and Tolerability of IHL-42X Compared to the Reference Drugs Phase 1
Recruiting NCT04547543 - Follow-up of Apneic Patients by Visio-consultation N/A
Recruiting NCT05371509 - Novel Myofunctional Water Bottle to Reduce OSA and Snoring Study N/A
Completed NCT02515357 - Mediterranean Diet/Lifestyle Intervention in Obstructive Sleep Apnea N/A
Completed NCT05582070 - Effect on Sleep of Surgical Treatment of Severe Nasal Obstruction N/A
Active, not recruiting NCT03189173 - Combined Upper-airway and Breathing Control Therapies for Obstructive Sleep Apnea Phase 2
Completed NCT04084899 - The Effect of CPAP on Lung Hyperinflation in Patients With OSA
Completed NCT03032029 - Registry on the Treatment of Central and Complex Sleep-Disordered Breathing With Adaptive Servo-Ventilation
Recruiting NCT04028011 - Clinical Evaluation of a Wearable Technology for the Diagnosis of Sleep Apnoea
Recruiting NCT06047353 - Community Health Advocates for Motivating PAP Use in Our Neighborhoods. N/A
Completed NCT05253963 - Acute Effect of CPAP on Weight in Patients With Obstructive Sleep Apnea N/A
Recruiting NCT06029959 - Stroke and CPAP Outcome Study 3 N/A
Recruiting NCT06150352 - Sleep Apnea, Neurocognitive Decline and Brain Imaging in Patients With Subjective or Mild Cognitive Impairment
Completed NCT03589417 - Postural Stability, Balance and Fall Risk in Patients With Obstructive Sleep Apnea
Recruiting NCT04335994 - ENhancing Outcomes in Cognitive Impairment Through Use of Home Sleep ApNea Testing N/A
Withdrawn NCT04063436 - Evaluation of a New Nasal Pillows Mask for the Treatment of Obstructive Sleep Apnea N/A
Recruiting NCT05385302 - Sociological Determinants of Positive Airway Pressure Adherence in OSA Patients
Recruiting NCT04572269 - Metabolomics of Obstructive Sleep Apnea
Not yet recruiting NCT06467682 - 12-week Tele-exercise Program in Patients With OSA N/A
Withdrawn NCT04011358 - Retinal Vein Occlusion and Obstructive Sleep Apnea: A Case Control Study N/A