Omeprazole 20 mg in Patients With Laryngopharyngeal reflux and Comorbid Chronic Rhinosinusitis
Primary Purpose
Laryngopharyngeal Reflux, Chronic Rhinosinusitis (Diagnosis)
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Omeprazole 20mg
Placebo oral capsule
Sponsored by
About this trial
This is an interventional treatment trial for Laryngopharyngeal Reflux focused on measuring omeprazole, placebo, treatment, adults
Eligibility Criteria
Inclusion Criteria:
- laryngopharyngeal reflux
- chronic rhinosinusitis
Exclusion Criteria:
- allergic rhinitis
- asthma
- cystic fibrosis
- nasal polyposis
- severe systemic diseases
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Treatment arm
Placebo arm
Arm Description
omeprazole 20 mg capsule once daily for 8 weeks
matching placebo capsules ones daily for 8 weeks
Outcomes
Primary Outcome Measures
Reduction in signs and symptoms of laryngopharyngeal reflux
Reflux symptom index (RSI) score
Reduction in signs and symptoms of laryngopharyngeal reflux
Reflux finding score (RFS)
Secondary Outcome Measures
Reduction of signs and symptoms of comorbid chronic rhinosinusitis
Nasal obstruction, anterior/posterior nasal drip, headache, sneezing, cough, smell and taste disorder with frequency and intensity of the symptoms was graded from 0 (no problem) to 3 (severe problem).
Nasal endoscopy with endoscopy scores were based on the assessment of nasal mucosa edema, secretions and presence of polyps and were graded from 0 (no problem) to 3 (severe problem).
Association of the severity of signs and symptoms of laryngopharyngeal reflux with the ones of chronic rhinosinusitis
Full Information
NCT ID
NCT03086070
First Posted
March 6, 2017
Last Updated
December 29, 2020
Sponsor
Children's Hospital Srebrnjak
Collaborators
University Hospital Center Sisters of Charity, Zagreb, Croatia, Belupo
1. Study Identification
Unique Protocol Identification Number
NCT03086070
Brief Title
Omeprazole 20 mg in Patients With Laryngopharyngeal reflux and Comorbid Chronic Rhinosinusitis
Official Title
Omeprazole 20 mg in Patients With Laryngopharyngeal reflux and Comorbid Chronic Rhinosinusitis - a Randomized, Double Blind, Placebo Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
January 1, 2010 (Actual)
Primary Completion Date
April 30, 2010 (Actual)
Study Completion Date
June 30, 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital Srebrnjak
Collaborators
University Hospital Center Sisters of Charity, Zagreb, Croatia, Belupo
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
Data Monitoring Committee
No
5. Study Description
Brief Summary
The hypothesis of this study is that a gastroesophageal reflux recommended treatment with proton pump inhibitor (dose and duration) compared to placebo significantly reduces both the signs and symptoms of laryngopharyngeal reflux and comorbid chronic rhinosinusitis. Primary objective was to determine whether 8 weeks of treatment with omeprazole 20 mg ones daily (OD) significantly reduces the signs and symptoms of laryngopharyngeal reflux when compared to placebo in patients with laryngopharyngeal reflux with comorbid chronic rhinosinusitis. Secondary objectives were to determine whether 8 weeks of treatment with omeprazole 20 mg OD significantly reduces the signs and symptoms of comorbid chronic rhinosinusitis in patients with laryngopharyngeal reflux when compared to matching placebo; and to investigate the association of the severity of signs and symptoms of laryngopharyngeal reflux with the ones of chronic rhinosinusitis in the same group of patients. The research was carried out as a double blind randomized placebo controlled trial. Patients were randomized into two groups in an approximate 1:1 ratio using a concealed random sequence. After randomization and initial assessment treatment was initialized. Patients on active treatment were given omeprazole 20 mg once daily half an hour before breakfast for 8 weeks, while those in the placebo group were given matching placebo tablets using the same regimen for 8 weeks as the group on the active treatment. Patients were reassessed at the end of treatment for signs and symptoms of laryngopharyngeal reflux and comorbid chronic rhinosinusitis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Laryngopharyngeal Reflux, Chronic Rhinosinusitis (Diagnosis)
Keywords
omeprazole, placebo, treatment, adults
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
randomized, double blind, placebo controlled trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment arm
Arm Type
Experimental
Arm Description
omeprazole 20 mg capsule once daily for 8 weeks
Arm Title
Placebo arm
Arm Type
Placebo Comparator
Arm Description
matching placebo capsules ones daily for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Omeprazole 20mg
Intervention Description
omeprazole 20 mg capsules were administered per os half an hour before breakfast for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Intervention Description
Matching placebo oral capsules were administered per os half an hour before breakfast for 8 weeks
Primary Outcome Measure Information:
Title
Reduction in signs and symptoms of laryngopharyngeal reflux
Description
Reflux symptom index (RSI) score
Time Frame
8 weeks
Title
Reduction in signs and symptoms of laryngopharyngeal reflux
Description
Reflux finding score (RFS)
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Reduction of signs and symptoms of comorbid chronic rhinosinusitis
Description
Nasal obstruction, anterior/posterior nasal drip, headache, sneezing, cough, smell and taste disorder with frequency and intensity of the symptoms was graded from 0 (no problem) to 3 (severe problem).
Nasal endoscopy with endoscopy scores were based on the assessment of nasal mucosa edema, secretions and presence of polyps and were graded from 0 (no problem) to 3 (severe problem).
Time Frame
8 weeks
Title
Association of the severity of signs and symptoms of laryngopharyngeal reflux with the ones of chronic rhinosinusitis
Time Frame
Baseline and after 8 weeks of treatment.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
laryngopharyngeal reflux
chronic rhinosinusitis
Exclusion Criteria:
allergic rhinitis
asthma
cystic fibrosis
nasal polyposis
severe systemic diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Srđan A Anzić, MD, PhD
Organizational Affiliation
Children's Hospital Srebrnjak
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Anonymised individual participant data can be obtained for other researchers on a written request to the principal investigator.
Citations:
PubMed Identifier
29024410
Citation
Anzic SA, Turkalj M, Zupan A, Labor M, Plavec D, Baudoin T. Eight weeks of omeprazole 20 mg significantly reduces both laryngopharyngeal reflux and comorbid chronic rhinosinusitis signs and symptoms: Randomised, double-blind, placebo-controlled trial. Clin Otolaryngol. 2018 Apr;43(2):496-501. doi: 10.1111/coa.13005. Epub 2017 Oct 23.
Results Reference
result
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Omeprazole 20 mg in Patients With Laryngopharyngeal reflux and Comorbid Chronic Rhinosinusitis
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