Drug-induced Sleep Endoscopy: a prediction tool for success rate of oral appliance treatment

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON20741

Enrollment

Registered

2020-03-03

Start date

2019-12-01

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea

Interventions

None

Eligibility

Inclusion criteria

Inclusion criteria: - Patients of 18 years and older with obstructive sleep apnea confirmed by poly(somno)graphy - Apnea-hypopnea index between 15 and 30 - BMI < 35

Exclusion criteria

Exclusion criteria: - Dentition not suitable for OAT - Other dental problems, e.g. temporomandibular dysfunction, micrognathia

Design outcomes

Primary

Measure	Time frame
Poly(somno)graphy 6 months after treatment (AHI, ODI 3%,..)	—

Secondary

Measure	Time frame
Quality of life: ESS and FOSQ-30 Patients’ complaints BMI Complications: temporomandibular dysfunction, dental problems,..	—

Contacts

Public ContactChristianne Veugen

Sint Antonius Hospital

c.veugen@antoniusziekenhuis.nl088-3202100

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)