Analysis of Impact on Nasal Obstruction by Commercially Available Internal Nasal Stents

Withdrawn before enrolling

Conditions studied: Nasal Obstruction

In brief

Commercially-available internal nasal stents placed inside the nostril should produce decreased nasal obstruction detectable subjectively (volunteers will fill out a survey) and objectively (degree of obstruction will be measured with a rhinomanometer which measure resistant of airflow while breathing through nose).

Key facts

Study ID

NCT00683254

Run by

Bethany L. Jones

People needed

0

Starts

2008-05-01

Expected to finish

2008-08-01

Last updated by the study team

2017-05-11

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 years or older

You may not qualify if…

• history of nasal surgery, currently using topical nasal steroid spray, over the counter decongestant, history of recurrent epistaxis or history of nosebleed within 2 weeks prior to data collection, currently pregnant

Where it is running

• University of Iowa Department of Otolaryngology — Iowa City, Iowa, United States

Full record on ClinicalTrials.gov

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