Clinical Trials Directory

Trials / Unknown

UnknownNCT04228016

Efficacy of an Intranasal Stent on Nasal Obstruction at Night

Efficacy of an Intranasal Stent on Nasal Obstruction at Night: A Prospective Multicenter Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
46 (estimated)
Sponsor
Centre Hospitalier Intercommunal Creteil · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aims to demonstrate a decrease with normalization of nasal resistance in the forward decubital position and with an intra-nasal stent in patients with nasal obstruction.

Detailed description

All patients consulting for nasal obstruction at night and who have functional nasal test with pathological resistance in decubitus position are included. Functional nasal test (non invasive tests) will be performed before and after intranasal introduction of a stent: anterior rhinomanometry to measure nasal function by the measure of resistance and acoustic rhinometry to measure the geometry of nasal fossa by the measure of minimal sectional cross area sitting, after 30 minutes of decubitus then new measurements with a stent in decubitus position in each nostril .

Conditions

Interventions

TypeNameDescription
DEVICEDevice: nastent™Patients with Nasal obstruction at night, will be used intrasal stent during 15 nights. These are flexible silicone tubes that are lubricated and easy to insert into the nasal cavities, which would restore the permeability of the nasal cavities.

Timeline

Start date
2019-09-27
Primary completion
2022-09-30
Completion
2023-09-30
First posted
2020-01-14
Last updated
2023-03-07

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT04228016. Inclusion in this directory is not an endorsement.