Effect on snoring and feasibility of Nasal Airway Stent

Effect on snoring and feasibility of Nasal Airway Stent - Effect and feasibility of Nasal Airway Stent

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000020662

Enrollment

Registered

2016-04-01

Start date

2016-04-01

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

Snoring

Interventions

Nasal Airway Stent 7 days

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Subjects who approve to take part in the study as examinees after informed consent

Exclusion criteria

Exclusion criteria: (1) Patient with sleep apnea syndrome undergoing medical treatment (2) Patient with severe respiratory diseases (3) Patient with severe liver, renal, heart, etc. diseases. (4) Subject who cannot insert Nasal Airway Stent into the nasal cavity (5) Subject who cannot perform examinations (6) Subject judged as inadequate by researcher

Design outcomes

Primary

Measure	Time frame
(1) feasibility of using Nasal Airway Stent Before and After 4 days using Nasal Airway Stent, assessed for 3 days about (2) snoring by digital voice recorder (3) apnea and hypopnea (AHI) by Apnea hypopnea testing apparatus	—

Countries

Japan

Contacts

Public ContactYuki Sumi

Tokyo Medical and Dental University School of health sciences, Faculty of Medicine. Biofunctional Informatics, Biomedical Laboratory Sci

ysumi.pulm@tmd.ac.jp03-5803-5372

Outcome results

None listed

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