Obstructive Sleep Apnea, Snoring
Conditions
Keywords
Snoring, Obstructive Sleep Apnea
Brief summary
Prospective Evaluation of a Palato-Pharyngeal Implant System (PPIS) for the Treatment of Snoring and Obstructive Sleep Apnea Syndrome (OSAS): A Pilot Study.
Detailed description
The clinical study is designed as single center, prospective, non-randomized and non-blinded clinical study. Since the surgical procedure is independent of the population a single center study is applied. A double-blind study is not possible considering the implantation procedure with the surgeon always knowing if the device is set. Therefore, the study is designed to be non-randomized and non-blinded as a pilot trial. To reduce bias and other influences of single surgeon skills a principal investigator and one investigator are part of the clinical study. Further, subjects with previous treatments such as Pillar implant or previous airway surgery other than nasal, adenoid, tonsil or UPPP are excluded from the clinical study. A double-blind study is not possible considering the implantation procedure with the surgeon always knowing if the device is set. Therefore, the study is designed to be non-randomized and non-blinded as a pilot trial.
Interventions
DEVICEImplantation
Implantation of 6 PPIS implants
Sponsors
Medartis AG
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Single center, prospective, non-randomized, and non-blinded study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* • Socially disturbing snoring and obstructive sleep apnea syndrome with AHI≥10/h * Predominantly retropalatal obstructions established either by: * Drug-induced sedation nasendoscopy * or ApneaGraph ≥60% (optional) * or successful application of the Velumount palatal device (optional) * Findings for predominantly retropalatal obstructions in ENT-examination: * No tonsils or tonsils grade I * Normal finding of larynx and tongue base, no omega-shaped epiglottis * No lingual tonsil hypertrophy * ASA (American Society of Anaesthesiology, 1963) classes I or II * Body mass index (BMI) \< 30 kg/m2 * Age \> 18 yrs * Fix bed partner * Ability to read and understand the patient's information
Exclusion criteria
* • Previous Pillar implants * Medartis palatinal implant (from previous phase I study) * Previous airway surgery other than nasal, adenoid, tonsil or UPPP * Presence of other sleep disorders * Psychiatric disorders * Neurological disorders (e.g. Cerebrovascular injury) * Dysmorphia of the cranial skeleton * Pregnancy or breastfeeding * Known hypersensitivity to nitinol * Participation in another clinical study * Recurrent tonsillitis with prescription of antibiotics during the last 2 years (≥3x/year) * Omega-shaped epiglottis * Lingual tonsil hypertrophy * Kinking of the internal carotid artery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| AHI reduction | 3 months post-op | AHI reduction |
Countries
Switzerland
Outcome results
None listed