Effect of the Mandibular Advancement Device on snoring: An evaluation based on objective acoustic Parameters

Effect of the Mandibular Advancement Device on snoring: An evaluation based on objective acoustic Parameters - Objective measurement of snoring

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00040349

Enrollment

Registered

2026-06-02

Start date

2018-01-01

Completion date

Unknown

Last updated

2026-06-22

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

Conditions

Obstruktive sleep apnoe and snoring

Interventions

Group 1: In patients with untreated obstructive sleep apnea (OSA) and concomitant snoring, integration a MAD (Mandibular Advancement Device) is performed to treat the underlying disease (OSA). In its

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Regular dental condition, Snoring

Exclusion criteria

Exclusion criteria: Jaw joint complaints, Reduced dental status

Design outcomes

Primary

Measure	Time frame
Objective evaluation of snoring by physical (sound pressure level, sound energy) and psychoacoustic parameters (loudness, roughness)	—

Secondary

Measure	Time frame
Determination of respiratory parameters (apnea-hypnea index and oxygen desaturation index, body measure index, sleep position)	—

Countries

Germany

Contacts

Public ContactRené Fischer

Universitätsklinikum Regensburg

rene.fischer@ukr.de+49 941 944 9401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 29, 2026