Trials / Withdrawn
WithdrawnNCT02123498
The Study of Eustachian Tube Dysfunction and Laryngopharyngeal Reflux
The Study of the Diagnosis of Eustachian Tube Dysfunction (ETD): Identifying the Relationship of Ear Fullness to Laryngopharyngeal Reflux (LPR)
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Loma Linda University · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to investigate the relationship between ear fullness, pressure, and/or pain and laryngopharyngeal reflux, in order to focus medical therapy and improve therapeutic outcomes in this patient population.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Omeprazole | 40mg, to be taken once daily by mouth, 30-60 minutes before meals, for at least 6 weeks |
| DRUG | Ranitidine | 300mg, to be taken once daily by mouth, before bedtime, for at least 6 weeks |
| DRUG | Pantoprazole | 40mg, to be taken twice daily by mouth, 30-60 minutes before meals, for at least 6 weeks. (Alternative intervention if participant cannot tolerate omeprazole, is on an anticoagulant medication, or if on medication contraindicated for omeprazole and ranitidine) |
| PROCEDURE | 24-Hour Diagnostic pH-Probe Test | Participants will undergo a routine clinical 24-hour diagnostic pH-probe test to assess quantitative measures for laryngopharyngeal reflux. |
| PROCEDURE | Laryngoscopy | Participants will undergo routine clinical laryngoscopy to assess presence of laryngopharyngeal reflux. |
Timeline
- Primary completion
- 2015-05-01
- First posted
- 2014-04-25
- Last updated
- 2016-09-26
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT02123498. Inclusion in this directory is not an endorsement.