Evaluation of mandibular advancement device with high compliance rate for obstructive sleep apnea patient

Evaluation of mandibular advancement device with high compliance rate for obstructive sleep apnea patient - Evaluation of mandibular advancement device with high compliance rate for obstructive sleep apnea patient

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000018643

Enrollment

Registered

2015-08-31

Start date

2015-08-31

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

obstructive sleep apnea syndrome

Interventions

teat with soft-type AMP device then treat with hard-type AMP device teat with hard-type AMP device then treat with soft-type AMP device

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Obstructive slepp apnea syndrome patient diagnosed by full polysomunography study 2. OSAS patients who need to treat of AMP device 3. >20 years of age

Exclusion criteria

Exclusion criteria: 1. Patients who has underwent other treatment for OSAS 2. Patients with central sleep apnea dominance (CAI >5/hr) 3. Patients with other sleep disorders 4. Patients with mental disorders 5. Patients with craniofacial disorders 6. Patients with multiple teeth loss

Design outcomes

Primary

Measure	Time frame
Usability of AMP device after using AMP devices for 2 weeks	—

Secondary

Measure	Time frame
Quality of sleep after using AMP diverse for 2 weeks	—

Countries

Japan

Contacts

Public ContactEri Makihara

Kyushu Dental University Division of Occlusion & Maxillofacial Reconstruction

maki-eri@kyu-dent.ac.jp093-582-1131

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026