Cystic Fibrosis With Other Manifestations, Sinusitis, Chronic
Conditions
Keywords
Chronic Rhinosinusitis (CRS), Cystic Fibrosis related CRS
Brief summary
Assess if the use of SYNRINSE can improve short-term subjective and objective outcome measures after one week in patients with active Chronic Rhinosinusitis (CRS) who have had prior sinus surgery.
Detailed description
SYNRINSE is osmotically balanced and also contains soluble chitosan-argininamide, a modified natural glycopolymer that has a number of properties important to relieving the symptoms of mucus build up and bacterial biofilms. First, SYNRINSE reduces the viscosity of biofilms, the protective environment of infective bacteria that prevents topical antibiotics and other rinses to penetrate to reach the bacterial. By disrupting biofilms, SYNRINSE allows them to be cleared from the sinuses. Second, SYNRINSE has been shown to interact with the polymers comprise mucus, loosening thick, sticky layers and reducing their ability to adhere together and to mucosal surfaces. Third, all of the components in SYNRINSE are biocompatible and soothing to sensitive nasal cavities.
Interventions
DRUGSynrinse
Non-CF Cohort The first 10 non-CF subjects will be instructed to once daily irrigate both nasal passages with SynRinse (supplied) delivered via nasal irrigation using the NeilMed® Sinus Rinse™ system for 1 week. The subjects will be asked to refrain from performing any sinus irrigations during the test treatment period with any product including saline. The second set of 10 non-CF subjects (if the study continues to this point) will be instructed to irrigate both nasal passages twice daily (rather than once daily) for one week with SynRinse (supplied). The subjects will be asked to refrain from performing any sinus irrigations during the test treatment period with any product including saline. CF Cohort The first 5 subjects in the CF cohort will irrigate with with SynRinse delivered via nasal irrigation using the NeilMed Sinus Rinse system for 1 week. The second set of 5 subjects with CF will irrigate both nasal passages twice daily for one week with SynRinse.
Sponsors
University of Washington
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Non-randomized, non-blinded single arm cohort study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* age \>= 18 * Meet diagnostic criteria for CRS (as defined by the AAO-HNS 2015 Clinical Practice Guidelines for Adult Sinusitis). * Have undergone at least one functional endoscopic sinus surgery, be at least 6 weeks out from surgery, be free of any complication from surgery, and have patent sinuses confirmed by nasal endoscopy. * Have active sinus disease as defined as purulent sinus discharge visualized on nasal endoscopy. * Have more than mild symptoms as determined by the SNOT-22 with a score \>20. * Be willing to hold off on standard therapy for chronic sinusitis for 1 week including oral antibiotics and/or oral steroids. * If on topical steroids for greater than 1 month (sprays, drops, or irrigation) these will be continued based on the patients' current use (continued if they are already on them, not initiated if they are not on them). * Must be able to irrigate with large volume/low pressure nasal lavage throughout the study.
Exclusion criteria
:• Have an allergy to shell fish. * Be able to return for follow up evaluation in 1 week (+ up to 5 days if needed) * Have obstructive nasal polyps * Participants who have used topical antibiotics within 4 weeks of treatment or are actively using them and unwilling to stop * Participants who have used systemic steroids within 4 weeks of treatment * Are unable to give informed consent or complete self-administered questionnaires written in English because of cognitive impairment, language barrier, or severe medical conditions. * Have a terminal illness or significant immune dysfunction. * Have severe or emergent complications from CRS or presence of a sinus tumor. * Patients with Cystic Fibrosis will be recruited in a parallel study. * Participants who are unwilling to discontinue other sinus irrigations treatments and steroid lavage if already on them (including baby shampoo, surfactant, colloid silver, manuka honey, iodine, alcohol, tea tree oil, or any other compound).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Sino-Nasal Outcome Test 22 (SNOT-22) | 1 week | Test pre-treatment SNOT-22 (sinusitis-specific quality of life) and compare to post-treatment SNOT-22 scores to measure any change in disease specific quality of life. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Sinus bacteria culture | 1 week | Obtain a pre-treatment endoscopic collected culture and a post-treatment endoscopic collected culture to see if the treatment impacts a pathogen detected in the pre-treatment culture. |
| Lund-Kennedy Endoscopy Score (LKES) | 1 week | Measure change in pre-treatment LKES and post-treatment LKES to determine if treatment impacts any change in the appearance of the patient's sinuses on endoscopy |
| Visual Analog Scale (VAS) | 1 week | Determine the tolerability of SYNRINSE as measured on a 10cm VAS |
| Future use questionnaire | 1 week | Record percentage of subjects willing to use SYNRINSE in the future |
Countries
United States
Outcome results
None listed