Skip to content

Determinants of Medical and Surgical Treatment Outcomes in Chronic Sinusitis

Determinants of Medical and Surgical Treatment Outcomes in Chronic Sinusitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01332136
Enrollment
966
Registered
2011-04-08
Start date
2011-04-30
Completion date
2016-03-31
Last updated
2016-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Rhinosinusitis

Brief summary

This research study will be completed by enrolling a prospective, observational cohort study to evaluate medical versus surgical treatment outcomes for chronic sinus disease. This investigation will compare quality of life outcomes between each treatment type, as well as measure cellular and molecular markers of inflammation in the sinus mucosa, to create models that predict improvement in quality of life following treatment.

Interventions

None listed

Sponsors

National Institute on Deafness and Other Communication Disorders (NIDCD)
CollaboratorNIH
Oregon Health and Science University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Adult (\>= 18 years) * Chronic rhinosinusitis as defined by the 2007 multi-disciplinary adult sinusitis guidelines * Able to complete all surveys/questionnaires in English * Persistent symptoms following initial medical management * Received at least 1 course of broad spectrum antibiotics or culture directed antibiotics for at least a total of 14 days * Received at least a 3 week trial of topical steroid sprays OR at least a 5 day trial of systemic corticosteroid therapy. * Counseled for subsequent treatment options including either medical management or endoscopic sinus surgery

Exclusion criteria

* Children (\<18 years) * Unable to complete all surveys/questionnaires at baseline

Design outcomes

Primary

MeasureTime frame
Disease-specific quality of life18 months post-treatment

Secondary

MeasureTime frame
General health-related quality-of-life18 months post-treatment
Olfaction18 months post-treatment

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026