Tongue Morphology and Posterior Airway Space as Predictors of Response in Patientswith Hypoglossal Nerve Stimulation Therapy

Sponsor
Cantonal Hosptal, Baselland (Other)
Overall Status
Recruiting
CT.gov ID
NCT06154577
Collaborator
Insel Gruppe AG, University Hospital Bern (Other)
54
2
11.5
27
2.3

Study Details

Study Description

Brief Summary

Hypoglossal nerve stimulation (HNS) plays an increasingly important role in managing patients with obstructive sleep apnea (OSA) who do not tolerate CPAP therapy and are not eligible for other alternative treatment options, such as mandibular advancement devices or positional therapy. The posterior upper airway space dimensions are crucial in managing patients with HNS in the patient selection process and therapy control. The lateral collapse of the upper airway is of crucial importance. Lateral collapse at the palatal level and of the oropharyngeal walls is a well-established negative predictive factor for therapeutic success. Patients with complete concentric collapse at the palatal level (pCCC) in drug-induced sedation endoscopy (DISE) must be excluded from the implantation of HNS, which is cumbersome and invasive. Endoscopy has the inherent limitation that only one level can be observed at a given time, and assessment is possibly hampered by phlegm.

During activation and titration of HNS, tongue protrusion is observed in the awake patient. However, this method does not allow for assessing the opening of the retroglossal (RG) and retropalatal (RP) airway space, which is the ultimate therapeutic goal. Insufficient opening of the airway is the reason for non-responders with HNS. Insufficient upper airway opening can be either at the retropalatal or retroglossal level. The study aims to identify insufficient airway openings better using sub-mental ultrasonography. Sub-mental standardized and orientated ultrasonography offers a quantitative, reproducible way of assessing transverse upper airway dimensions and anatomic features of the upper airway in a rapid and non-invasive manner. In addition, anatomic characteristics of the airway's adjacent tissue, such as the size and shape of the tongue, may also have an impact on the effectiveness of HNS. Tongue morphology and posterior airway space assessment could be used in preoperative evaluation and during therapeutic titration of HNS. The clinical routine could be included tongue morphology and posterior airway space assessment without additional patient risks. However, the clinical value of assessing posterior airway space and tongue morphology in patients with HNS is yet unknown.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Ultrasonography

Study Design

Study Type:
Observational
Anticipated Enrollment :
54 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Tongue Morphology and Posterior Airway Space as Predictors of Response in Patientswith Hypoglossal Nerve Stimulation Therapy
Actual Study Start Date :
May 15, 2023
Anticipated Primary Completion Date :
Apr 30, 2024
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Obstructive sleep apnea patients

39 obstructive sleep apnea patients with hypoglossal nerve stimulation

Diagnostic Test: Ultrasonography
Assessment of tongue morphology and posterior airway space using ultrasonography (AmCAD-UO, CE mark NB1639)

Healthy controls

15 healthy control participants

Diagnostic Test: Ultrasonography
Assessment of tongue morphology and posterior airway space using ultrasonography (AmCAD-UO, CE mark NB1639)

Outcome Measures

Primary Outcome Measures

  1. Prediction of therapeutic success with hypoglossal nerve stimulation [Most recent sleep testing before examination after HNS implantation, a maximum of 6 months before examination]

    Success is defined as apnea-hypopnea index in the most recent sleep testing ≤ 20/h and 50% reduction from baseline

Secondary Outcome Measures

  1. Prediction of AHI reduction, defined as the difference between pre- and postoperative AHI, with HNS based on tongue morphology and posterior airway space. [Most recent sleep testing before examination after HNS implantation, a maximum of 6 months before examination]

    AHI reduction is defined as apnea-hypopnea index in the most recent sleep compared to the baseline value before HNS implantation

  2. Comparison of pharyngeal dimensions between visual assessment and tongue morphology and posterior airway space [through study completion, from 15.05.2023 to 14.05.2024]

    Visual assessment is performed both by DISE and wake transnasal endoscopy. Tongue morphology and posterior airway space is analyzed using ultrasonography

  3. Therapeutical guidance using tongue morphology and posterior airway space to identify the obstructing upper airway segment compared to wake fiberoptic endoscopy during HGS in non-responders. [through study completion, from 15.05.2023 to 14.05.2024]

    Changes to therapeutic HNS settings during study visit

  4. Patient comfort rated by the patients for wake transnasal endoscopy and sub-mental ultrasonography [through study completion, from 15.05.2023 to 14.05.2024]

    Rated on a visual analog scale (VAS) from 0 to 10 (0 meaning no discomfort; 10 meaning very uncomfortable

  5. Information gain through from tongue morphology and posterior airway space imaging [through study completion, from 15.05.2023 to 14.05.2024]

    Rating by the physician if the additional information gained from tongue morphology and posterior airway space imaging at functional stimulation threshold is a valuable adjunct to the oral observation of tongue protrusion rated on a VAS

  6. Comparison of pharyngeal dimensions of healthy and patients with OSA and HNS [through study completion, from 15.05.2023 to 14.05.2024]

    Pharyngeal dimensions measured using ultrasonography

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients older than 18 year

  • patients with a hypoglossal nerve implantation

  • control group: 15 subjects without OSA (AHI<10/h)

  • written informed consent

  • sufficient knowledge of German or French to understand informed consent

Exclusion Criteria:
  • Patients younger than 18 years

  • unwillingness to give informed consent

  • incapable of performing Müller's maneuver

  • history of head and neck surgery other than HNS, tonsillectomy, and maxillomandibular advancement

  • diagnosis of congestive heart failure or chronic pulmonary disease

  • diagnosis of co-morbid sleep disorders, including central sleep apnea

  • pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kantonsspital Baselland Liestal Baselland Switzerland 4410
2 University Hospital Bern, Inselspital Bern Switzerland 3010

Sponsors and Collaborators

  • Cantonal Hosptal, Baselland
  • Insel Gruppe AG, University Hospital Bern

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cantonal Hosptal, Baselland
ClinicalTrials.gov Identifier:
NCT06154577
Other Study ID Numbers:
  • 2023-00117
First Posted:
Dec 4, 2023
Last Update Posted:
Dec 4, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Cantonal Hosptal, Baselland
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 4, 2023