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Clinical Trials/ISRCTN16919107
ISRCTN16919107
Completed
Not Applicable

Clinical and laryngoscopic predictors of symptomatic response to pantoprazole magnesium in patients with newly diagnosed laryngopharyngeal reflux: a prospective study

Takeda Pharmaceutical Company Limited0 sites100 target enrollmentAugust 17, 2016
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ConditionsLaryngopharyngeal refluxaryngopharyngeal refluxDigestive System

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laryngopharyngeal reflux
Sponsor
Takeda Pharmaceutical Company Limited
Enrollment
100
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 17, 2016
End Date
TBD
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Aged 18 years and over
  • •2\. Chief complaint of hoarseness, sore throat, throat burning/pain, throat clearing, voice loss, cough, excessive throat mucus, globus, or choking for at least 4 weeks in the preceding 3 months

Exclusion Criteria

  • •1\. Patients younger than age 18
  • •2\. Patients with identifiable laryngeal pathology
  • •3\. Upper respiratory tract infection in the past 4 weeks
  • •4\. Identifiable allergic causes of laryngitis
  • •5\. Previous laryngeal malignancy, surgery or radiotherapy
  • •6\. Women of childbearing potential not using an effective contraceptive method
  • •7\. Acid\-suppressive therapy within the past 4 weeks
  • •8\. Hypersensitivity to the active ingredient, or to any of the excipients of the product
  • •9\. Patients taking HIV protease inhibitors or methotrexate

Outcomes

Primary Outcomes

Not specified

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