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Saline Irrigation After Surgery in Patients With Chronic Sinusitis (HVSI)

Primary Purpose

Chronic Rhinosinusitis

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
NeilMed sinus rinse
Salinex
Sponsored by
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Rhinosinusitis focused on measuring saline irrigation, chronic rhinosinusitis, endoscopic sinus surgery, high volume saline irrigation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Documented diagnosis of unilateral or bilateral CRS
  • Documented failed medical treatment of CRS
  • Eighteen (18) to sixty-five (65) years of age
  • Planned ESS for the treatment of CRS
  • Able to read and understand English

Exclusion criteria:

  • Pregnant
  • Cystic Fibrosis
  • Diagnosed immotile cilia syndrome
  • Diagnosed immunodeficiency syndrome
  • Diagnosed fungal sinusitis
  • Sinonasal tumours or obstructive lesions

Sites / Locations

  • University of Calgary Otolaryngology - Head & Neck Surgery
  • Western University Dept. of Otolaryngology - Head & Neck Surgery
  • Ottawa University Otolaryngology - Head & Neck Surgery
  • Mount Sinai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

High volume saline irrigation

Placebo

Arm Description

Patients in this group will receive high volume saline irrigation (NeilMed sinus rinse)

Patients in this group will receive low volume saline irrigation (Salinex)

Outcomes

Primary Outcome Measures

Sinonasal Outcomes Scale (SNOT-22)
Subjective scale, completed by patient. Validated scale for chronic sinusitis.
Lund MacKay score
Objective scale, validated, completed by investigator. Preoperative CT scan is scored based on degree of sinus opacification (0-24).
Nasal and Sinus Symptom Score (NSS) - Subjective scale
A subjective scale, filled out by the patient, specific to symptoms of sinusitis.
Perioperative Sinus Endoscopy scale (POSE)
Objective scale, completed by treating physician, to assess sinonasal contents endoscopically. Validated scale.

Secondary Outcome Measures

Full Information

First Posted
April 1, 2012
Last Updated
April 22, 2014
Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Collaborators
NeilMed Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT01575223
Brief Title
Saline Irrigation After Surgery in Patients With Chronic Sinusitis
Acronym
HVSI
Official Title
The HVSI STUDY: High Volume Saline Irrigation in the Post-operative Management of Chronic Rhinosinusitis: A Multicenter Randomized Single-Blind Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
April 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Collaborators
NeilMed Pharmaceuticals

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Purpose: To determine if high volume saline nasal irrigation (HVSI), (NeilMed® Sinus Rinse™) offers a benefit over low volume saline irrigation (LVSI), (Salinex®) in the early post-operative management in patients with chronic rhino sinusitis.
Detailed Description
Background: Chronic Rhinosinusitis (CRS) is a common inflammatory condition of the upper respiratory tract lasting more than 8 to 12 weeks. Major symptoms include facial congestion/fullness, facial pain/pressure, nasal obstruction/blockage, purulent nasal drainage, and reduction or loss of smell. The diagnosis must include two major symptoms and either endoscopic evidence of polyps, edema or mucopurulent discharge from the middle meatus and/or CT changes in the mucosa of sinuses or osteomeatal complexes.1 CRS has an estimated prevalence of 5% in the Canadian population2, and up to 16% in some adult populations in the United States.3 Sinusitis is associated with a major societal health care burden, costing billions of dollars a year in North America.4,5 The medical treatment of CRS includes topical saline and corticosteroid sprays, systemic steroids and antimicrobials. Specifically, saline nasal irrigation (SNI) is a safe, nonpharmacologic treatment, and an important and efficacious component in the management of CRS.6,7 SNI can vary by concentration (e.g. hypertonic, isotonic, hypotonic) and device (e.g. bulb syringe, nasal mist, squeeze bottle). The Mayo Clinic recently reviewed major expert consensus guidelines on the medical treatment of CRS.8 Although they recognized an overall paucity of controlled trials for any medical treatment, and a lack of a consensus or algorithm in the treatment of CRS, there is an overall consensus agreement of the use for SNI in this population. In this review, there was no mention of treatment of CRS in postoperative period, and no recommendation of what type of SNI is best. Few studies examine various SNI formulations in the postoperative period. These were highlighted by Canadian authors in a recent exhaustive review of SNI in sinusitis.9 Three studies, all greater than 15 years old, include formulations that are not currently in popular use, or even available in North America.10-12 These did show that pressurized jets or sprays of seawater were more effective than nasal drops. More recently, Harvey et al. examined how irrigation is delivered and retained in the sinus, using more common devices.13,14 In a cadaveric model, they compared HVSI to LVSI devices and found a greater delivery (p<..02) in the former. To date there are no studies comparing HVSI to LVSI, using subjective patient benefit and objective endoscopic measure outcomes, in the postoperative CRS patient. One study did examine two different SNI devices in the management of CRS.15 The authors recruited 150 subjects with CRS in the primary care setting, and randomized them to two weeks of SNI with a bulb syringe, SNI with a nasal irrigation pot, and a control group of reflexology massage.15 Hypertonic saline was used in both treatment groups. Subjective questionnaires were administered at baseline and at the end of the study period. Both groups significantly improved, with no significant difference between the two SNI devices. Patients equally preferred the two devices. Popular HVSI and LVSI formulations with patients and physicians are NeilMed® Sinus Rinse™ and Salinex®, respectively. These are two examples of positive pressure treatments,13 which have enjoyed widespread usage in North America preceding sufficient evidence-based medicine demonstrating safety and efficacy. This is likely because topical saline sprays are considered safe; they do not require a prescription, and perhaps most importantly the massive marketing campaign surrounding SNI devices. SNI devices have received significant news coverage and appearances on major television shows, including the Oprah Winfrey Show, the New York Times, and numerous YouTube videos.16 Purpose: The authors hypothesize that there is an advantage of HVSI over LVSI. The mechanical effect of high volume irrigation helps ensure that a larger surface area of sinonasal mucosa is debrided and cleansed. The aim of this study is to determine if there is a clinical benefit of HVSI over LVSI in the postoperative period in patients with CRS. This information would help otolaryngologists, family physicians, and other health care professionals recommend the best SNI device for their patients with CRS. It would also provide a much-needed prospective and controlled trial in the evidence for SNI in CRS in the post-operative period. Population/Procedure: This is a multicenter, randomized, single blind, controlled prospective study evaluating the subjective and objective outcomes of HSVI versus LSVI in patients who have ESS for CRS. One month postoperative scores will be compared to preoperative scores. The expected total number of patients to be enrolled in this study is approximately 100, with a planned completion time of one year. At our institution, ten patients who are offered endoscopic sinus surgery (ESS) for CRS will be approached for study participation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Rhinosinusitis
Keywords
saline irrigation, chronic rhinosinusitis, endoscopic sinus surgery, high volume saline irrigation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
86 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High volume saline irrigation
Arm Type
Active Comparator
Arm Description
Patients in this group will receive high volume saline irrigation (NeilMed sinus rinse)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients in this group will receive low volume saline irrigation (Salinex)
Intervention Type
Device
Intervention Name(s)
NeilMed sinus rinse
Intervention Description
High volume saline irrigation
Intervention Type
Device
Intervention Name(s)
Salinex
Intervention Description
Low volume saline irrigation
Primary Outcome Measure Information:
Title
Sinonasal Outcomes Scale (SNOT-22)
Description
Subjective scale, completed by patient. Validated scale for chronic sinusitis.
Time Frame
One month post-operatively
Title
Lund MacKay score
Description
Objective scale, validated, completed by investigator. Preoperative CT scan is scored based on degree of sinus opacification (0-24).
Time Frame
1 month postoperatively
Title
Nasal and Sinus Symptom Score (NSS) - Subjective scale
Description
A subjective scale, filled out by the patient, specific to symptoms of sinusitis.
Time Frame
1 month post-operatively
Title
Perioperative Sinus Endoscopy scale (POSE)
Description
Objective scale, completed by treating physician, to assess sinonasal contents endoscopically. Validated scale.
Time Frame
1 month post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Documented diagnosis of unilateral or bilateral CRS Documented failed medical treatment of CRS Eighteen (18) to sixty-five (65) years of age Planned ESS for the treatment of CRS Able to read and understand English Exclusion criteria: Pregnant Cystic Fibrosis Diagnosed immotile cilia syndrome Diagnosed immunodeficiency syndrome Diagnosed fungal sinusitis Sinonasal tumours or obstructive lesions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian J Witterick, MD MSc FRCSC
Organizational Affiliation
Samuel R Lunenfeld Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary Otolaryngology - Head & Neck Surgery
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T5J 3E4
Country
Canada
Facility Name
Western University Dept. of Otolaryngology - Head & Neck Surgery
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 3K7
Country
Canada
Facility Name
Ottawa University Otolaryngology - Head & Neck Surgery
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4E9
Country
Canada
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2N2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
21658337
Citation
Desrosiers M, Evans GA, Keith PK, Wright ED, Kaplan A, Bouchard J, Ciavarella A, Doyle PW, Javer AR, Leith ES, Mukherji A, Robert Schellenberg R, Small P, Witterick IJ. Canadian clinical practice guidelines for acute and chronic rhinosinusitis. J Otolaryngol Head Neck Surg. 2011 May;40 Suppl 2:S99-193. English, French.
Results Reference
background
PubMed Identifier
12838019
Citation
Chen Y, Dales R, Lin M. The epidemiology of chronic rhinosinusitis in Canadians. Laryngoscope. 2003 Jul;113(7):1199-205. doi: 10.1097/00005537-200307000-00016.
Results Reference
background
PubMed Identifier
15174752
Citation
Anand VK. Epidemiology and economic impact of rhinosinusitis. Ann Otol Rhinol Laryngol Suppl. 2004 May;193:3-5. doi: 10.1177/00034894041130s502.
Results Reference
background
PubMed Identifier
10069873
Citation
Ray NF, Baraniuk JN, Thamer M, Rinehart CS, Gergen PJ, Kaliner M, Josephs S, Pung YH. Healthcare expenditures for sinusitis in 1996: contributions of asthma, rhinitis, and other airway disorders. J Allergy Clin Immunol. 1999 Mar;103(3 Pt 1):408-14. doi: 10.1016/s0091-6749(99)70464-1.
Results Reference
background
PubMed Identifier
19932850
Citation
Harvey RJ, Debnath N, Srubiski A, Bleier B, Schlosser RJ. Fluid residuals and drug exposure in nasal irrigation. Otolaryngol Head Neck Surg. 2009 Dec;141(6):757-61. doi: 10.1016/j.otohns.2009.09.006.
Results Reference
background

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Saline Irrigation After Surgery in Patients With Chronic Sinusitis

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