Status:

COMPLETED

Laryngopharyngeal Reflux and Proton Pump Inhibitor (PPI) Treatment

Lead Sponsor:

University of Utah

Collaborating Sponsors:

PriCara, Unit of Ortho-McNeil, Inc.

Conditions:

Laryngopharyngeal Reflux

Eligibility:

All Genders

18+ years

Phase:

PHASE2

PHASE3

Brief Summary

This study proposes to investigate prospectively, the presence of molecular markers for inflammation in laryngopharyngeal reflux (LPR) patients and to study the effect of a proton pump inhibitor (Acip...

Detailed Description

Objectives: This study proposes to investigate prospectively, the presence of molecular markers for inflammation in LPR patients and to study the effect of a proton pump inhibitor on these molecular ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • The subject group will consist of 25 subjects who have untreated LPR diagnosed by laryngoscopic assessment and 24-hour pH probe.

Exclusion

    Key Trial Info

    Start Date :

    August 1 2003

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    May 1 2006

    Estimated Enrollment :

    24 Patients enrolled

    Trial Details

    Trial ID

    NCT00204698

    Start Date

    August 1 2003

    End Date

    May 1 2006

    Last Update

    January 16 2008

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    University of Utah

    Salt Lake City, Utah, United States, 84132

    Laryngopharyngeal Reflux and Proton Pump Inhibitor (PPI) Treatment | DecenTrialz