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Xylitol for Chronic Sinusitis

Primary Purpose

Chronic Rhinosinusitis, Rhinosinusitis, Sinusitis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Xylitol
Saline
Sponsored by
Ochsner Health System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Rhinosinusitis focused on measuring chronic rhinosinusitis, chronically draining sinus, condemned sinus, post-endoscopic sinus surgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Ochsner Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Xylitol

Control

Arm Description

This arm will evaluate the effect of topical xylitol therapy on biofilm production with the use of PCR bacterial sequencing before and after medical intervention.

This arm is the standard of care saline irrigation solution.

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Sino-Nasal Outcome Test-22 (SNOT-22)
Maximum score of 110 points based on responses to 22 questions
Brief Smell Identification Test (BSIT)
Total scores range from 0 to 12; higher scores indicate greater olfactory function
Endoscopic appearance of the patient's sinuses in response to the use of topical xylitol
Correlation of DNA seqeuncing results with conventional sinonasal cultures

Full Information

First Posted
July 21, 2017
Last Updated
April 6, 2023
Sponsor
Ochsner Health System
Collaborators
Tulane University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03229551
Brief Title
Xylitol for Chronic Sinusitis
Official Title
Xylitol Topical Irrigation for Treatment of Recalcitrant Chronic Sinusitis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
July 16, 2018 (Actual)
Study Completion Date
July 16, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ochsner Health System
Collaborators
Tulane University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
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.
Detailed Description
Problem Statement: The purpose of this investigation is to conduct a trial within a subgroup of difficult-to-treat patients with CRS. This difficult group of patients will have undergone an exhaustive surgical and medical treatment of CRS These patient often will be frustrated with the lack of improvement in their symptoms despite maximal medical and surgical therapy. The effectiveness of topical surfactants is a research gap in treating CRS but has promising correlates in other medical fields. Purpose of Study/Potential Impact: 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. Potential Benefits: Topical xylitol could potentially decrease CRS symptoms, leading to improvements in patient quality of life. This decrease could potentially lead to fewer visits to primary care physicians/otolaryngologists. These could lead to less antibiotics, radiographs being obtained and unnecessary surgical procedures being performed, all of which could potentially reduce the burden of medical expenditure in the treatment of this disease. Potential Risks: Potential risks are minimal but include a sweet aftertaste in the mouth and burning in the nose; which have been reported in previous studies. Hypothesis: 5% (wt/vol) Xylitol saline irrigation into the diseased paranasal sinus, as a part of a post-ESS refractory CRS management plan, will reduce biofilm formation in the sinus and result in symptomatic relief in affected patients. General Design: A prospective, randomized, double-blinded experimental design will be utilized. Patients will be randomized into the xylitol-saline treatment arm versus the control saline arm. Concurrent corticosteroid/antibiotic therapy will be utilized in both arms based on results of bacterial DNA sequencing. Patients will undergo weekly in-office irrigations for three weeks and will be evaluated one month and three months post-treatment. The postoperative care will be standardized across all participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Rhinosinusitis, Rhinosinusitis, Sinusitis, Drain Sinus, Endoscopic Sinus Surgery, Biofilms, Bacterial Overgrowth
Keywords
chronic rhinosinusitis, chronically draining sinus, condemned sinus, post-endoscopic sinus surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Xylitol
Arm Type
Experimental
Arm Description
This arm will evaluate the effect of topical xylitol therapy on biofilm production with the use of PCR bacterial sequencing before and after medical intervention.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
This arm is the standard of care saline irrigation solution.
Intervention Type
Drug
Intervention Name(s)
Xylitol
Intervention Description
Topical 5% Xylitol (wt/vol) diluted in saline nasal irrigant. Topical corticosteroid and antibiotic as directed by bacterial DNA sequencing results will be diluted in this irrigant and administered concurrently.
Intervention Type
Drug
Intervention Name(s)
Saline
Intervention Description
Saline as a standard-of-care nasal irrigant. Topical corticosteroid and antibiotic as directed by bacterial DNA sequencing results will be diluted in this irrigant and administered concurrently.
Primary Outcome Measure Information:
Title
The effect of topical xylitol therapy on biofilm production with the use of PCR bacterial sequencing before and after medical intervention.
Description
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.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Sino-Nasal Outcome Test-22 (SNOT-22)
Description
Maximum score of 110 points based on responses to 22 questions
Time Frame
3 months
Title
Brief Smell Identification Test (BSIT)
Description
Total scores range from 0 to 12; higher scores indicate greater olfactory function
Time Frame
3 months
Title
Endoscopic appearance of the patient's sinuses in response to the use of topical xylitol
Time Frame
3 months
Title
Correlation of DNA seqeuncing results with conventional sinonasal cultures
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
Ochsner Medical Center
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data will be presented in either a paper or electronic format. Upon its arrival, it will immediately be de-identified. If presented in a paper format, it will immediately be transferred into an electronic database. Only key personnel will have access to this data. The data will be encrypted and stored on permanent hardware or within the Ochsner secure network on a password-protected workstation.
Citations:
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Citation
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Xylitol for Chronic Sinusitis

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