Efficacy of Lansoprazole in Chronic Post Nasal Drip (PND)
Larynx Disease
About this trial
This is an interventional treatment trial for Larynx Disease
Eligibility Criteria
Inclusion Criteria: Negative RAST inhalant allergy panel OR negative skin testing (Group A) Positive RAST or Positive skin testing AND insufficient response to all of the following: (Group B) Allergen avoidance Topical nasal steroids Allergy shots if indicated Antihistamines Negative CT sinuses (coronal) < 4mm of mucosal thickening and < 3 sinus sites Absence of air-fluid levels Negative anterior rhinoscopy Absence of pus, crusts on mucosal surfaces Exclusion Criteria: Age < 18 Pregnancy, confirmed by urine pregnancy test at day of randomization Ciliary dyskinesia Immune deficiency Cystic fibrosis Diagnosis of acute sinusitis or chronic RS (AAO-HNS) Active use of topical decongestant Use of PPI within the last 30 days Previous fundoplication Uncontrolled thyroid disease Isolated chronic cough without the symptom of post nasal drip
Sites / Locations
- Vanderbilt University Medical Center, Vanderbilt Digestive Disease Clinic, TVC, Room 1660
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Lansoprazole
Sugar Pill