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NCT01282125 Clinical Trial

Nasal Obstruction in Sleep Apnea Patients Compared to the General Population

Nasal Obstruction Clinical Trial

Official title:
A Comparative Study of Nasal Obstruction in a Sleep Apnea Population Compared to the General Population

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01282125
Other study ID # OSAS og nasalstenose
Secondary ID
Status Completed
Phase N/A
First received January 18, 2011
Last updated March 10, 2017
Start date December 2010
Est. completion date November 2016

Study information
Verified date March 2017
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Recent clinical findings of research at Trondheim University Hospital suggest that surgical correction of the nose septum in addition to volume reduction of the nose cavity may be beneficial in patients who suffer from both nose obstruction and obstructive sleep apnea syndrome(data not yet published).

This study aims to compare nose obstruction prevalence in sleep apnea patients and the general population

Recruitment information / eligibility
Status Completed
Enrollment 217
Est. completion date November 2016
Est. primary completion date November 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- ???

Exclusion Criteria:

- ???

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Norway St Olavs Hospital Trondheim University Hospital Trondheim

Sponsors (2)
Lead Sponsor Collaborator
Norwegian University of Science and Technology Sorlandet Hospital HF

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Moxness MH, Bugten V, Thorstensen WM, Nordgård S, Bruskeland G. A comparison of minimal cross sectional areas, nasal volumes and peak nasal inspiratory flow between patients with obstructive sleep apnea and healthy controls. Rhinology. 2016 Dec 1;54(4):34 — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary patient reported nasal obstruction assessed by a 10-point visual analogue scale (VAS) and Sino Nasal Outcome Score(SNOT-20) questionnaire. 1 week
Primary objective nasal obstruction measured by acoustical rhinometry and Peak Nasal Inspiratory Flow (PNIF). 1 week
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