Sinusitis Clinical Trial
Official title:
Xylitol Topical Irrigation for Treatment of Recalcitrant Chronic Sinusitis
Verified date | April 2023 |
Source | Ochsner Health System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this investigation is to conduct a randomized controlled trial within a subgroup of difficult-to-treat patients with CRS, evaluating the use of topical xylitol treatment concurrently with topical steroid/antibiotics combination in the effort to disrupt biofilms and improve disease control. The effectiveness of topical surfactants is a research gap in treating CRS but has promising correlates in other medical fields. Specifically, the investigators will be studying the effect of topical xylitol therapy on biofilm production with the use of PCR bacterial sequencing before and after medical intervention.
Status | Completed |
Enrollment | 1 |
Est. completion date | July 16, 2018 |
Est. primary completion date | July 16, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult patients above the age of 18 - History of chronic rhinosinusitis history who had undergone bilateral endoscopic sinus surgery to include at a minimum maxillary antrostomy and anterior ethmoidectomy. - Continued chronic sinusitis that is refractory to medical therapy after surgical intervention Exclusion Criteria: - Patients under age of 18 - Non-English speaking - History of immunodeficiency disease - Cystic fibrosis - Primary ciliary dyskinesia - History of granulomatous disease - Active smoker - Treatment with antifungal medications - Use of antifungal medications - Acute bacterial infection requiring antibiotics - Active pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Ochsner Medical Center | New Orleans | Louisiana |
Lead Sponsor | Collaborator |
---|---|
Ochsner Health System | Tulane University School of Medicine |
United States,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The effect of topical xylitol therapy on biofilm production with the use of PCR bacterial sequencing before and after medical intervention. | Bacterial DNA sequencing obtained via endoscopic swab will be performed pre-treatment to analyse the presence of biofims in the diseased sinus. This assay will be repeated from the same sinus post-treatment with 5% Xylitol (wt/vol) to evaluate if medical intervention decreases biofilm production in the diseased sinus. | 3 months | |
Secondary | Sino-Nasal Outcome Test-22 (SNOT-22) | Maximum score of 110 points based on responses to 22 questions | 3 months | |
Secondary | Brief Smell Identification Test (BSIT) | Total scores range from 0 to 12; higher scores indicate greater olfactory function | 3 months | |
Secondary | Endoscopic appearance of the patient's sinuses in response to the use of topical xylitol | 3 months | ||
Secondary | Correlation of DNA seqeuncing results with conventional sinonasal cultures | 3 months |
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