A Post-marketing Surveillance of the Negative Pressure Sleep Therapy System to Treat Obstructive Sleep Apnea

Somnics

Status: Unknown

Conditions: Obstructive Sleep Apnea (OSA)

Treatments: Device: iNAP® Sleep Therapy System (iNAP)

Study type: Interventional

Funder types: Industry

Identifiers

NCT02698059

iNAP®-CE-1501

Details and patient eligibility

About

This is a post-marketing surveillance study to investigate the efficacy and safety of the Negative Pressure Sleep Therapy System for the treatment of obstructive sleep apnea.

Full description

This is a multi-center, two-stage, single-arm, prospective, first-night order cross-over, evaluator-blind, post-marketing surveillance study to evaluate the efficacy, safety and tolerance of the iNAP® Sleep Therapy System (iNAP), a tongue and soft palate retaining intraoral device, in adults with obstructive sleep apnea (OSA).

Enrollment: 63 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 1. Female or male adults with age between 18~65 years old. (S1)
• 2. Non-obese patients with body mass index (BMI) <29 kg/m2. (S1)
• 3. Patients able to read and sign on the informed consent form and able to comply with study requirements. (S1)
• 4. Patients able to be properly fitted* with the oral interface as observed by the device feasibility test. (S1)
• 5. Patients with oxygen desaturation index (ODI) between 10~40 (S2).

• 6. Patients with oral negative vacuum time maintained* by iNAP® ≥4 hours/night and total sleep time (TST) ≥4 hours/night (S3).

  • iNAP® pressure more negative than -30 mmHg will be considered evidence of effective oral appliance application.
• 7. Patients with apnea-hypopnea index (AHI) between 10~40 and TST ≥4 hours/night (Baseline PSG Night).

• 8. Patients with oral negative vacuum time maintained* by iNAP® ≥4 hours/night and TST ≥4 hours/night (1st Tx PSG Night).

  • iNAP® pressure more negative than -30 mmHg will be considered evidence of effective oral appliance application.

Exclusion criteria

• 1. Patients who are allergic to silicone.
• 2. Patients with obstructed nasal passages as evidenced by the inability to breathe through the nose with the mouth closed.
• 3. Patients who recently experienced a near-miss or prior automobile accident due to sleepiness.
• 4. Patients who have or have had hypoxemia (SpO2 <80%) in the past six months caused by diseases other than OSA such as cardiac disease or severe pulmonary/respiratory disorders such as chronic obstructive pulmonary disease (COPD), interstitial lung disease, pneumothorax, pneumonia, etc.
• 5. Female patients who are lactating, pregnant or intend to become pregnant during the study period.
• 6. Patients with primary insomnia or any concomitant diagnosed or suspected sleep disorder.

• 7. Patients with muscle disease, central nervous disease or chronic neurological disorders, including central sleep apnea*.

  • Central sleep apnea is defined as a central apnea index (CAI) ≥ 5/hr or if central sleep apnea accounts for ≥ 50% of the total AHI.
• 8. Patients in whom it is not suitable to use iNAP® in the opinion of the Investigator including, but not limited to, alcohol or substance abuse, loose teeth, missing teeth, or grinding teeth, completed deviated septum (Type IV or VII) or completed closed nostrils or advanced periodontal disease or tonsillar volumes greater than grade 3.
• 9. Patients with an inability to sleep through the night including, but not limited to, menopausal hot flashes, working at nights or rotating night shifts, planned travel across four or more time zones during the study period or within one week prior to study participation, or a sleep schedule not compatible with study site practices.
• 10. Patients with potential complications of sleep apnea that, in the opinion of the Investigator, may affect the study interpretation or the health or safety of the patients including, but not limited to, narcolepsy, restless leg syndrome, nasopharyngeal carcinoma (NPC), end stage renal failure, a history of severe cardiovascular disease (including New York Heart Association (NYHA) class III or IV cardiac failure, coronary artery disease with angina or myocardial infarction/stroke in the past six months, uncontrolled hypertension or hypotension or cardiac arrhythmias), unstable heart or renal transplantation or use of medicine or other treatment(s) that may confound the result of the study or pose additional risks to the patient, such as oral anticoagulants or other agents making patients prone to tongue hemorrhage.

Stage II Inclusion Criteria:

Patients who fulfill all the enrollment criteria of Stage I and whose treated AHI on the 1st Tx PSG Night is below 40.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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63 participants in 2 patient groups

Treated

Experimental group

Description:

iNAP® Sleep Therapy System Treatment

Treatment:

Device: iNAP® Sleep Therapy System (iNAP)

Baseline/Control

No Intervention group

Description:

Self-controlled, pre-treatment baseline