Investigation of the Association Between Nasal Polyposis and Extraesophageal Reflux Disease
Primary Purpose
Nasal Polyps, Gastroesophageal Reflux
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
lansoprazole
Sponsored by
About this trial
This is an interventional treatment trial for Nasal Polyps focused on measuring Nasal polyps, Gastroesophageal Reflux
Eligibility Criteria
Inclusion Criteria: Subjects will: Be adults with nasal polyposis recruited from the PI's private practice Not be currently taking a PPI Be able and willing to undergo a noninvasive 24 hour pH probe study; and Take a PPI. Exclusion Criteria: Patients who: Are pregnant Have a history of surgical treatment for reflux disease History of allergic or adverse reaction to Prevacid or adverse reaction to Prevacid during the study period; and Do not meet inclusion criteria.
Sites / Locations
- Head and Neck Surgery Associates
Outcomes
Primary Outcome Measures
Presence of Reflux in Patients With Polyposis
Presence of Laryngopharyngeal reflux was measured by 24 hour pH impedance probe monitor per equipment manufacturer software. Two or more episodes in twenty four hours was considered positive, in accordance with published standards.
Secondary Outcome Measures
Full Information
NCT ID
NCT00215787
First Posted
September 15, 2005
Last Updated
September 21, 2010
Sponsor
Head and Neck Surgery Associates
1. Study Identification
Unique Protocol Identification Number
NCT00215787
Brief Title
Investigation of the Association Between Nasal Polyposis and Extraesophageal Reflux Disease
Official Title
Investigation of the Association Between Nasal Polyposis and Extraesophageal Reflux Disease
Study Type
Interventional
2. Study Status
Record Verification Date
September 2010
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Head and Neck Surgery Associates
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Although nasal polyposis has been recognized as an inflammatory process for many years, the true etiology of nasal polyposis mainly unknown. Despite surgical removal, the recurrence rate after surgery has been reported as high as 87% within the first year after surgery. Anecdotally the Principal Investigator found an incidence of pH probe-proven laryngopharyngeal reflux approaching 80% in his patients with nasal polyposis. Although his number of cases was small, the incidence of recurrence of polyps in these patients was 17%.
The PI believes that such an association is too great to be explained by chance alone, and deserves further study. He anticipates two contributions to the literature from this study, the first documenting the incidence of extraesophageal (laryngopharyngeal) reflux in patients with polyposis, and the second showing the impact of reflux treatment on the recurrence rate of the polyps, initially after one year of therapy.
Detailed Description
Although nasal polyposis has been recognized as an inflammatory process for many years, the true etiology of nasal polyposis mainly unknown. Despite surgical removal, the recurrence rate after surgery has been reported as high as 87% within the first year after surgery. Anecdotally the Principal Investigator found an incidence of pH probe-proven laryngopharyngeal reflux approaching 80% in his patients with nasal polyposis. Although his number of cases was small, the incidence of recurrence of polyps in these patients was 17%.
The PI believes that such an association is too great to be explained by chance alone, and deserves further study. He anticipates two contributions to the literature from this study, the first documenting the incidence of extraesophageal (laryngopharyngeal) reflux in patients with polyposis, and the second showing the impact of reflux treatment on the recurrence rate of the polyps, initially after one year of therapy.
Eligible patients found to have nasal polyps will be offered the chance to participate in this study. They will undergo non-invasive pH probe monitoring for 24 hours. If extraesophageal (laryngopharyngeal) reflux is discovered, they will be provided (at no cost) proton pump inhibitor medication (PPI), prescribed in accordance with published standards in the otolaryngology literature. Their polyposis will be treated as any other patient presenting with polyposis; participation in the study will not affect the course of polyp treatment. The incidence of recurrence will be monitored and recorded over the first year after treatment.
Included: Subjects will be adults with nasal polyposis, recruited from the PI's private practice, will not be currently taking a PP!, will be able and willing to undergo a noninvasive 24 hour pH probe study, and willing to take a PPI. Excluded: patients who are pregnant, have a history of surgical treatment for reflux disease, history of allergic or adverse reaction to Prevacid or adverse reaction to Prevacid during the study period, and those not meeting inclusion criteria.
In addition to routine office otolaryngology examination, subjects will undergo noninvasive 24 hour esophageal pH probe monitoring. The probe is swallowed and placed in the same manner as a feeding tube. The procedure is done in the office. No sedation is required, but the mucosa may be sprayed with topical 4% lidocaine for comfort. This procedure is the standard for diagnosis of extraesophageal (laryngopharyngeal) reflux, and will be performed in accordance with manufacturer guidelines
Risks include temporary dysphagia while the probe is in place, and nasal irritation. Mild, self-limited epistaxis has been rarely reported
The procedure will be done within manufcturer guidelines under direct vision. Topical Afrin may be used to control any mild epistaxis. Topical 4% lidocaine will be applied to minimize dysphagia. These steps have proven very affective in minimizing these risks.
If the study hypothesis is correct, the patient may have an diminished risk of recurrence of their nasal polyposis. If the patient is found to have previously undiagnosed reflux disease, this will allow it to be treated appropriately. Undiagnosed/untreated reflux has been associated with multiple medical problems including laryngeal and esophageal cancer. The patient will be given their PPI medication free of charge for the duration of the study. The noninvasive pH probe study will be done free of charge. No direct monetary payment will be given to participants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasal Polyps, Gastroesophageal Reflux
Keywords
Nasal polyps, Gastroesophageal Reflux
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
lansoprazole
Other Intervention Name(s)
Prevacid is the brand name for this drug
Intervention Description
Lansoprazole 30 mg BID for 1 year
Primary Outcome Measure Information:
Title
Presence of Reflux in Patients With Polyposis
Description
Presence of Laryngopharyngeal reflux was measured by 24 hour pH impedance probe monitor per equipment manufacturer software. Two or more episodes in twenty four hours was considered positive, in accordance with published standards.
Time Frame
one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Subjects will:
Be adults with nasal polyposis
recruited from the PI's private practice
Not be currently taking a PPI
Be able and willing to undergo a noninvasive 24 hour pH probe study; and
Take a PPI.
Exclusion Criteria:
Patients who:
Are pregnant
Have a history of surgical treatment for reflux disease
History of allergic or adverse reaction to Prevacid or adverse reaction to Prevacid during the study period; and
Do not meet inclusion criteria.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott E Phillips, MD
Organizational Affiliation
Head and Neck Surgery Associates
Official's Role
Principal Investigator
Facility Information:
Facility Name
Head and Neck Surgery Associates
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46250
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
11030275
Citation
Vento SI, Ertama LO, Hytonen ML, Wolff CH, Malmberg CH. Nasal polyposis: clinical course during 20 years. Ann Allergy Asthma Immunol. 2000 Sep;85(3):209-14. doi: 10.1016/S1081-1206(10)62468-4.
Results Reference
background
PubMed Identifier
6988929
Citation
Virolainen E, Puhakka H. The effect of intranasal beclomethasone dipropionate on the recurrence of nasal polyps after ethmoidectomy. Rhinology. 1980 Mar;18(1):9-18.
Results Reference
background
PubMed Identifier
12353429
Citation
Postma GN, Johnson LF, Koufman JA. Treatment of laryngopharyngeal reflux. Ear Nose Throat J. 2002 Sep;81(9 Suppl 2):24-6.
Results Reference
background
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Investigation of the Association Between Nasal Polyposis and Extraesophageal Reflux Disease
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