Impact of Budesonide Irrigations on Patients With Chronic Rhinosinusitis and Impact on Sinus Surgery Rates

Withdrawn before enrolling · Phase 2/Phase 3

Conditions studied: Chronic Sinus Infection, Chronic Sinusitis, Chronic Sinusitis - Ethmoidal, Posterior, Chronic Sinus Congestion

In brief

This study is intended to assess the impact of a 90 day course of high volume budesonide irrigations for patients who have failed other medical therapy and assessing the impact of the budesonide irrigations on the need for sinus surgery.

Key facts

Study ID

NCT03519061

Run by

Kaiser Permanente

People needed

0

Starts

2019-08-13

Expected to finish

2019-10-01

Last updated by the study team

2021-01-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• adult (>18 yo)
• symptoms consistent with sinusitis for at least 12 weeks,
• undergone maximal medical therapy, including: extended course of antibiotics (21 days minimum), use of topical corticosteroids for a minimum of 6 weeks, use of saline rinses at least once a day for a minimum of 3 weeks
• CT showing evidence of chronic sinusitis.

You may not qualify if…

• pregnant women,
• age below 18,
• presence of nasal polyps or other nasal masses,
• failure to complete medical therapy,
• normal CT scan,
• intolerance to budesonide or saline irrigations via squeeze bottle (high volume, high flow).

Where it is running

• Kaiser Permanante Orange County — Irvine, California, United States

Full record on ClinicalTrials.gov

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