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Comparison of Nasal Steroids After FESS in CRSwNP

Primary Purpose

Sinusitis, Nasal Polyps

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
fluticasone nasal spray
Budesonide head upright
Budesonide head forward
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sinusitis focused on measuring Chronic rhinosinusitis with polyps, Nasal steroids, Functional endoscopic sinus surgery, SNOT-22, Lund-Kennedy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients who have had FESS for CRSwNP within the study period

Exclusion Criteria:

  1. Patients who are under the age of 18
  2. Concurrent oral corticosteroid use of the equivalent of greater than 10 mg of prednisone use per day
  3. The use of medications that accelerate the clearance of systemic cortisol (Dilantin, rifampin, amphetamines, and lithium)
  4. The use of medications that inhibit the clearance of systemic cortisol (ketoconazole, amphotericin B, bupropion, fluoroquinolones)
  5. Known hypersensitivity to corticosteroids
  6. A personal history of Wegener's Granulomatosis or other autoimmune disease with nasal manifestations

Sites / Locations

  • Yale Physicians Bldg
  • Yale ENT Stratford

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

fluticasone nasal spray

budesonide respule in head upright

budesonide head forward

Arm Description

Group one will be prescribed fluticasone nasal spray ( to use 2-50 mcg sprays to each nostril two times per day)

Group two will be prescribed budesonide respules (0.5 mg/2mL) to instill into each nostril in the upright position two times per day

Group three will be prescribed budesonide respules (0.5 mg/2mL) to use instill into each nostril in the head forward position two times per day with their head angled downwards by having their head lean forward off the side of a bed.

Outcomes

Primary Outcome Measures

SNOT-22 Scores
SNOT22 is a validated scale which measures sinonasal symptoms for sinusitis patients. The 22 questions are rated on a scale of 0-5 for a maximum total score of 110. Higher scores represent more symptomatic patients.

Secondary Outcome Measures

Lund-Kennedy Scoring for Nasal Endoscopy
The Lund Kennedy scoring system for nasal endoscopy rates the severity of the sinusitis based on the endoscopic appearance of the nasal mucosa. Edema, secretions and the presence of polyps are rated from 0-2, for a total maximum score of 6 per each side of the nose. Higher scores represent more severe disease.

Full Information

First Posted
July 15, 2014
Last Updated
January 12, 2018
Sponsor
Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT02194062
Brief Title
Comparison of Nasal Steroids After FESS in CRSwNP
Official Title
A Comparison of Budesonide Nasal Irrigation in Different Head Positions and Fluticasone Nasal Spray in Post-operative Functional Endoscopic Sinus Surgery Patients With Chronic Rhinosinusitis With Nasal Polyposis
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare intranasal fluticasone spray with budesonide nasal saline rinses in both the upright and head forward positions in patients who have had functional endoscopic sinus surgery (FESS) for chronic rhinosinusitis with nasal polyposis (CRSwNP) and measure differences in Sinonasal Outcome Test-22 (SNOT-22) scores and Lund- Kennedy scores on rigid nasal endoscopy at time points 1 week, 3 weeks, 6 weeks, 2 months, 4 months, and 6 months post-op.
Detailed Description
Chronic rhinosinusitis (CRS) is an inflammatory condition of the lining of the nose and sinuses that lasts 12 weeks or longer with objective evidence of mucosal inflammation (1). CRSwNP is characterized by the presence of bilateral nasal polyps in the middle meatus. Patients with CRSwNP for whom medical therapy has failed, often have functional endoscopic sinus surgery. Nasal steroids are important post-operatively to prevent polyps from recurring. Many studies have shown that nasal steroids are superior to placebo in maintaining improvement in symptom scores, such as SNOT-22, post-operatively by preventing polyps from returning (2). Nasal steroids can reduce inflammation locally and can prevent disease relapse without the systemic effects of oral steroids. However, there is no consensus as to which nasal steroid and which delivery method is most effective in treating these patients. Traditional nasal sprays, such as fluticasone spray, may not deliver the medication widely in the nasal cavity. Budesonide is available in a respule form that can be used to instill the medication in the nose. In an attempt to more effectively deliver the medication, changes in patient's head position has been prescribed to achieve better delivery (3). The safety of intranasal budesonide, a more potent steroid than fluticasone, has been established (4, 5). However, any improved efficacy over fluticasone nasal spray remains anecdotal as head to head comparisons have not previously been performed. Practice patterns among rhinologists in the post-operative prescription of nasal steroids vary widely. Determining which medication/delivery method is more effective will help rhinologists better treat their patients and prevent symptoms, for which the surgery was performed, from returning.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sinusitis, Nasal Polyps
Keywords
Chronic rhinosinusitis with polyps, Nasal steroids, Functional endoscopic sinus surgery, SNOT-22, Lund-Kennedy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
fluticasone nasal spray
Arm Type
Active Comparator
Arm Description
Group one will be prescribed fluticasone nasal spray ( to use 2-50 mcg sprays to each nostril two times per day)
Arm Title
budesonide respule in head upright
Arm Type
Active Comparator
Arm Description
Group two will be prescribed budesonide respules (0.5 mg/2mL) to instill into each nostril in the upright position two times per day
Arm Title
budesonide head forward
Arm Type
Active Comparator
Arm Description
Group three will be prescribed budesonide respules (0.5 mg/2mL) to use instill into each nostril in the head forward position two times per day with their head angled downwards by having their head lean forward off the side of a bed.
Intervention Type
Drug
Intervention Name(s)
fluticasone nasal spray
Other Intervention Name(s)
fluticasone propionate nasal, Flonase
Intervention Description
use 2-50 mcg sprays to each nostril two times per day
Intervention Type
Drug
Intervention Name(s)
Budesonide head upright
Other Intervention Name(s)
budesonide, pulmicort respules
Intervention Description
(0.5 mg/2mL) to instill into each nostril in the upright position two times per day
Intervention Type
Drug
Intervention Name(s)
Budesonide head forward
Other Intervention Name(s)
budesonide, pulmicort respules
Intervention Description
(0.5 mg/2mL) to instill into each nostril in the head forward position two times per day
Primary Outcome Measure Information:
Title
SNOT-22 Scores
Description
SNOT22 is a validated scale which measures sinonasal symptoms for sinusitis patients. The 22 questions are rated on a scale of 0-5 for a maximum total score of 110. Higher scores represent more symptomatic patients.
Time Frame
6 months post-op.
Secondary Outcome Measure Information:
Title
Lund-Kennedy Scoring for Nasal Endoscopy
Description
The Lund Kennedy scoring system for nasal endoscopy rates the severity of the sinusitis based on the endoscopic appearance of the nasal mucosa. Edema, secretions and the presence of polyps are rated from 0-2, for a total maximum score of 6 per each side of the nose. Higher scores represent more severe disease.
Time Frame
6 months post-op

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients who have had FESS for CRSwNP within the study period Exclusion Criteria: Patients who are under the age of 18 Concurrent oral corticosteroid use of the equivalent of greater than 10 mg of prednisone use per day The use of medications that accelerate the clearance of systemic cortisol (Dilantin, rifampin, amphetamines, and lithium) The use of medications that inhibit the clearance of systemic cortisol (ketoconazole, amphotericin B, bupropion, fluoroquinolones) Known hypersensitivity to corticosteroids A personal history of Wegener's Granulomatosis or other autoimmune disease with nasal manifestations
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R. Peter Manes, MD
Organizational Affiliation
Yale University School of Medicine, Asst Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale Physicians Bldg
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06510
Country
United States
Facility Name
Yale ENT Stratford
City
Stratford
State/Province
Connecticut
ZIP/Postal Code
06614
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22469599
Citation
Fokkens WJ, Lund VJ, Mullol J, Bachert C, Alobid I, Baroody F, Cohen N, Cervin A, Douglas R, Gevaert P, Georgalas C, Goossens H, Harvey R, Hellings P, Hopkins C, Jones N, Joos G, Kalogjera L, Kern B, Kowalski M, Price D, Riechelmann H, Schlosser R, Senior B, Thomas M, Toskala E, Voegels R, Wang de Y, Wormald PJ. EPOS 2012: European position paper on rhinosinusitis and nasal polyps 2012. A summary for otorhinolaryngologists. Rhinology. 2012 Mar;50(1):1-12. doi: 10.4193/Rhino12.000.
Results Reference
background
PubMed Identifier
23710959
Citation
Snidvongs K, Kalish L, Sacks R, Sivasubramaniam R, Cope D, Harvey RJ. Sinus surgery and delivery method influence the effectiveness of topical corticosteroids for chronic rhinosinusitis: systematic review and meta-analysis. Am J Rhinol Allergy. 2013 May-Jun;27(3):221-33. doi: 10.2500/ajra.2013.27.3880.
Results Reference
background
PubMed Identifier
19379619
Citation
Beule A, Athanasiadis T, Athanasiadis E, Field J, Wormald PJ. Efficacy of different techniques of sinonasal irrigation after modified Lothrop procedure. Am J Rhinol Allergy. 2009 Jan-Feb;23(1):85-90. doi: 10.2500/ajra.2009.23.3265.
Results Reference
background
PubMed Identifier
19128710
Citation
Bhalla RK, Payton K, Wright ED. Safety of budesonide in saline sinonasal irrigations in the management of chronic rhinosinusitis with polyposis: lack of significant adrenal suppression. J Otolaryngol Head Neck Surg. 2008 Dec;37(6):821-5.
Results Reference
background
PubMed Identifier
19289711
Citation
Sachanandani NS, Piccirillo JF, Kramper MA, Thawley SE, Vlahiotis A. The effect of nasally administered budesonide respules on adrenal cortex function in patients with chronic rhinosinusitis. Arch Otolaryngol Head Neck Surg. 2009 Mar;135(3):303-7. doi: 10.1001/archoto.2008.555.
Results Reference
background
PubMed Identifier
26679480
Citation
Neubauer PD, Schwam ZG, Manes RP. Comparison of intranasal fluticasone spray, budesonide atomizer, and budesonide respules in patients with chronic rhinosinusitis with polyposis after endoscopic sinus surgery. Int Forum Allergy Rhinol. 2016 Mar;6(3):233-7. doi: 10.1002/alr.21688. Epub 2015 Dec 17.
Results Reference
derived

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Comparison of Nasal Steroids After FESS in CRSwNP

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