[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"obstructive-sleep-apnoea-osa\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:obstructive-sleep-apnoea-osa":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,74],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100623439","feasibility-of-upper-airway-stimulation-in-osa-100623439",false,"NCT07396649","Feasibility of Upper Airway Stimulation in OSA","Feasibility of Non-invasive Electrical Nerve Stimulation of the Upper Airway in Patients With Obstructive Sleep Apnoea","Inclusion Criteria:\n\n* Obstructive sleep apnoea diagnosis with an AHI of 15-50 events\u002Fhour recorded in the baseline polysomnography (PSG)\n* BMI \\\u003C 32 kg\u002Fm²\n* Age \\> 18 years old\n* Able to read, write, and speak Dutch with acceptable visual and auditory acuity\n* Able and willing to provide informed consent\n\nExclusion Criteria:\n\n* Presence of a cardiac pacemaker or implantable cardiac defibrillator or ventriculoperitoneal shunt\n* Central (non-obstructive) AHI episodes \\>5 events\u002Fhour recorded in the baseline PSG\n* Inability to sleep supine\n* Pregnancy\n* Inability to undergo DISE\n* Inability or unwillingness to shave under and around their chin and neck if appropriate\n* Known inability to complete PSG with a total sleep time of \\> 4 hours\n* The use of other neurostimulatory devices\n* A diagnosis of periodic leg movement disorder\n* Awake resting arterial oxygen saturation \\\u003C93% (suggesting possible hypoventilation)\n* Unstable, untreated coronary or peripheral artery disease\n* Severe arterial hypertension defined as a resting blood pressure (BP) of \\>180\u002F110mmHg\n* Currently employed as a professional driver\n* Any previous sleep-related driving accident\n* A past or current condition that in the opinion of the investigator contraindicates enrolment (e.g. chronic substance abuse, severe psychiatric disorders)","ALL","19 Years",{"count":19,"type":20},15,"ESTIMATED","INTERVENTIONAL",[23],"NA","Project Breathe 1 is a short-duration (5 month) pilot investigation to assess the safety and tolerability of non-invasive electrical stimulation in adults with obstructive sleep apnoea. The investigation is an unblinded, uncontrolled, single arm design.",[26],"Obstructive Sleep Apnoea (OSA)",[28,29,30],"obstructive sleep apnoea","OSA","sleep apnoea","RECRUITING","2026-02-05",{"date":34,"type":35},"2026-02-09","ACTUAL",{"date":37,"type":35},"2026-01-29",{"date":39,"type":20},"2026-07",{"name":41,"class":42},"Notos Medical Limited","INDUSTRY",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":55,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":43},"100623897","sleep-disordered-breathing-database-100623897","NCT07402603","Sleep-disordered Breathing Database","Enhancing Patient Care: Sleep and Ventilation Database","Inclusion Criteria:\n\n* Age \\>18 years\n* Referred to Royal Free London NHS Foundation Trust Sleep and Ventilation Service\n* Agreed to undertake a sleep study\n\nExclusion Criteria:\n\n* Inability to consent",true,"18 Years",{"count":54,"type":20},5000,"5 Years","OBSERVATIONAL","The goal of this study is to collect clinical data on patients who have had a sleep study and are given a diagnosis of a sleep related breathing disorder such as obstructive sleep apnoea. Collecting this data in an organised way will mean that the investigators can monitor patients and their health outcomes.",[26,59],"Hypoventilation Syndrome",[61,62],"database","observational","NOT_YET_RECRUITING","2026-02-04",{"date":66,"type":35},"2026-02-11",{"date":68,"type":20},"2026-01-15",{"date":70,"type":20},"2036-01",{"name":72,"class":73},"Royal Free Hospital NHS Foundation Trust","OTHER",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":21,"phases":84,"briefSummary":85,"conditions":86,"keywords":87,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":43},"100613660","a-study-assessing-adult-patients-referred-to-an-nhs-sleep-service-with-suspected-obstructive-sleep-apnoea-this-study-aims-to-compare-the-sunrise-wearable-diagnostic-device-performance-and-potential-inclusion-in-a-nhs-diagnostic-pathway-with-oximetry-and-watchpat-which-are-currently-used-100613660","NCT07269483","A Study Assessing Adult Patients Referred to an NHS Sleep Service With Suspected Obstructive Sleep Apnoea. This Study Aims to Compare the Sunrise Wearable Diagnostic Device Performance and Potential Inclusion in a NHS Diagnostic Pathway With Oximetry and WatchPAT Which Are Currently Used.","Sunrise in Obstructive Sleep Apnoea Study (SOSA) A Comparison of the Sunrise Mandibular Movement Monitoring Device With Overnight Oximetry and WatchPAT in the Diagnosis and Management of Obstructive Sleep Apnoea.","SOSA","Inclusion Criteria:\n\n* • Adults (aged ≥18 years old) referred with suspected Obstructive Sleep Apnoea\n\n  * Patient has capacity to provide informed consent\n  * Patient has access to a smartphone with Bluetooth and WiFi or internet data to download the Sunrise app and to transmit the Sunrise results to the Sunrise portal. UHBW Trust Wi-Fi available to the patient at equipment collection and return if needed.\n  * Willing and able to comply with the study-specific procedures\n  * Ability to read and comprehend English or understand simple device user instructions with guided pictures in English.\n\nExclusion Criteria:\n\n* • Suspected diagnosis of a sleep disorder other than OSA (including central sleep apnoea, parasomnias, narcolepsy, idiopathic hypersomnia)\n\n  * Suspected chronic hypercapnic respiratory failure (history of acute hypercapnic respiratory failure, raised CO2 or serum bicarbonate)\n  * Patients with unstable cardiovascular disease or non-arteritic anterior ischaemic optic neuropathy\n  * Patients with beards who are unwilling to shave the area below their lip (the soul patch)\n  * Patients with conditions affecting the rotation of the condyle in the temporo-mandibular joint\n  * Unable to consent or lacks capacity to provide informed consent\n  * In-patient referrals\n  * Unwilling or unable to comply with the study-specific procedures.\n  * Patients who have requested in their medical notes not to be involved in research or not to receive digital communication",{"count":83,"type":20},100,[23],"The goal of this clinical trial is to evaluate whether the Sunrise device (that measure small jaw movements) can improve the diagnosis and management of Obstructive Sleep Apnoea (OSA) in adults (≥ 18 years) referred to a Sleep Clinic.\n\nThe main question it aims to answer are:\n\n\\- Does Sunrise lead to a higher proportion of definitive management decisions (initiate OSA treatment, discharge from the sleep clinic service, additional diagnostic testing required or a clinic appointment) compared to current screening practices, which includes either overnight oximetry or use of a wearable device called WatchPAT 300?\n\nResearchers will compare Sunrise results with oximetry and WatchPAT 300 outcomes to see if Sunrise improves diagnostic efficiency, reduces time to a diagnosis or clinical decision and enhances patient experience.\n\nParticipants will:\n\n* Follow the standard clinical pathway (oximetry or WatchPAT 300)\n* Use the Sunrise device simultaneously for one night with their usual test\n* Complete a patient feedback questionnaire on ease of use and experience\n* Return all equipment two days later, Sunrise results will not affect their clinical care and will be used for the study only",[26],[88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110],"Obstructive Sleep Apnoea","Home-testing devices for Obstructive Sleep Apnoea","sleep-disordered breathing","Excessive daytime sleepiness","Sunrise device","WatchPAT 300","Overnight oximetry","wearable sleep diagnostic device","Home sleep study","mandibular movement monitoring","diagnostic accuracy study","single-centre study","digital health technology","patient experience","patient feedback","NHS innovation","waiting list reduction","machine learning in sleep medicine","Home-testing devices for diagnosing obstructive sleep apnoea hypopnoea syndrome NICE guidance 2024","diagnostic pathway efficiency","Obstructive Sleep Apnoea Hypopnoea syndrome","patient reported outcomes","cost effectiveness","2025-12-12",{"date":113,"type":35},"2025-12-19",{"date":115,"type":35},"2025-07-28",{"date":117,"type":20},"2026-09-30",{"name":119,"class":73},"Virginia Hawkins"]