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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
Children's Hospital Srebrnjak
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Laryngopharyngeal Reflux focused on measuring omeprazole, placebo, treatment, adults

Eligibility Criteria

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

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

    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
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    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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