Severe Label Expansion for EVO Products Trial

Overview

Title: Severe Label Expansion for EVO Positioner (SLEEP) Study Description: Single-arm study to determine the safety and effectiveness of treating severe obstructive sleep apnea using the EVO Sleep and Snore Device (ProSomnus Sleep Technologies, Pleasanton, CA). Objectives: To determine the safety and effectiveness of the EVO Sleep and Snore Device in individuals with severe obstructive sleep apnea. Endpoints: The primary effectiveness endpoint is the Sher criteria defined as a reduction of Apnea-Hypopnea Index (AHI) of at least 50% from the baseline value and a post-treatment AHI of less than 20 events/hour at 6 months following initiation of Oral Appliance Therapy (OAT) titration. AHI will be collected using HSAT at baseline and 6 months. The primary safety objective is to evaluate safety by summarizing all reported device and/or procedure related adverse events from the time the EVO device is introduced through 6 months. Study Population: A maximum of 49 individuals over the age of 18 years with severe obstructive sleep apnea will be enrolled. Description of Sites/Facilities Enrolling Participants: The study will be conducted at up to four sites, up to two of which could be located outside of the US. Description of Study Device: The study device is the EVO Sleep and Snore Device (ProSomnus Sleep Technologies, Pleasanton, CA). The device is a mandibular repositioning device used to treat obstructive sleep apnea. The device is currently cleared for the treatment of mild and moderate OSA. Study Duration: The time from when the study opens to enrollment until completion of data analyses is estimated to be 15 months.

Interventions

• Device EVO Sleep and Snore Device
  ProSomnus EVO Sleep and Snore Device mandibular advancement device

Primary outcome measures

• Sher responder rate endpoint [Time frame: 6 months]
• Incidence of adverse events [Time frame: 6 months]

Secondary outcome measures (7)

• Sleep apnea-specific hypoxic burden [Time frame: 6 months]
• Epworth Sleepiness Scale change from baseline [Time frame: 6 months]
• Sher criteria responder rate point estimate [Time frame: 6 months]
• Severity classification change [Time frame: 6 months]
• Apnea-hypopnea index change from baseline [Time frame: 6 months]
• Oxygen desaturation index change from baseline [Time frame: 6 months]
• Sleep apnea-specific hypoxic burden change from baseline [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

• Provision of signed and dated informed consent form
• Stated willingness to comply with all study procedures and availability for the duration of the study
• Male or female, aged 18-80 years (inclusive)
• Diagnosed with uncomplicated severe OSA (AHI > 30 h-1); where uncomplicated is defined by the absence of:

• Conditions that place the patient at increased risk of non-obstructive sleep-disordered breathing (e.g., central sleep apnea, hypoventilation, and sleep-related hypoxemia \[e.g., resulting from severe chronic obstructive, interstitial lung disease, or pulmonary hypertension\]). Examples of such conditions include significant cardiopulmonary disease (congestive heart failure, recurrent atrial fibrillation, coronary artery disease, resistant hypertension), potential respiratory muscle weakness due to neuromuscular conditions, history of stroke, and chronic opiate medication use.
• Concern for significant non-respiratory sleep disorder(s) that require evaluation (e.g., disorders of central hypersomnolence, parasomnias, sleep-related movement disorders) or interfere with accuracy of HSAT (e.g., severe insomnia).
• Environmental or personal factors that preclude the adequate acquisition and interpretation of data from HSAT.
• Body mass index (BMI) < 35 kg/m2
• Absence of severe oxyhemoglobin desaturation during sleep, indicated by mean nocturnal SpO2 > 87%
• Adequate mandibular range of motion
• Adequate dentition

Exclusion criteria

An individual who meets any of the following criteria will be excluded from participation in this study:

• Inability to breathe through the nose comfortably
• Presence of > 25% CSA
• Presence of positional OSA per Amsterdam Positional OSA Classification I definition
• History of surgery intended to alter anatomy for the correction of OSA

• E.g., uvulopalatopharyngoplasty (UPPP), maxillomandibular advancement (MMA), tongue/hyoid suspension, slow maxillary expansion
• History of surgery intended to restore normal anatomy, such as tonsillectomy, adenoidectomy, septoplasty, or polypectomy, is permitted.
• Presence of hypoglossal nerve stimulation device (active or inactive)
• Use of CPAP or OAT within the two weeks prior to the baseline sleep study
• History of OAT that has been confirmed to provide effective therapy within the two years prior to the baseline sleep study
• Anticipated change in medical therapy during the study protocol that could alter OSA severity (e.g., weight loss surgery, weight loss drug, UPPP, MMA, tongue/hyoid suspension, etc.)
• Loose teeth or advanced periodontal disease
• History of temporomandibular joint disorder
• Resistant hypertension, defined as inadequately controlled blood pressure despite therapy with

≥ 3 oral hypertensive agents

• Use of pacemaker or other life-supporting device
• Participation in other studies that could interfere with the study protocol
• Pregnancy or lactation
• In the opinion of the investigator, unsuitable for inclusion in the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

United States · 2 centers

• Mount Sinai Integrative Sleep Center — New York
• Star Sleep and Wellness — Dallas

Identifiers

NCT: NCT07090395 · SP-005

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗