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Efficacy of Lansoprazole in Chronic Post Nasal Drip (PND)

Primary Purpose

Larynx Disease

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Lansoprazole Tablet
PH and impedence testing
manometry
lansoprazole
placebo
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Larynx Disease

Eligibility Criteria

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

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

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Lansoprazole

Sugar Pill

Arm Description

Outcomes

Primary Outcome Measures

Post Nasal Drainage Symptom Response
The primary outcome measure was postnasal drainage symptom response measured by using a visual analogue scale. At 8 and 16 weeks, a horizontal symptoms scale from 0% (no change) to 100% (symptoms completely resolved) was presented to participants to assess improvement in postnasal drainage symptoms.

Secondary Outcome Measures

Rhinosinusitis Outcome Measure(RSOM-31)
RSOM-31 includes 31 questions combined into a total score ranging from 0 to 155 with higher scores representing greater disease burden. Values are based on patient report.
Sino Nasal Outcome Test (SNOT-20)
SNOT-20 includes 20 questions combined into a total score ranging from 0 to 100 with higher numbers representing greater rhinosinusitis health burden and represents patient-reported symptom severity.
Quality of Life Questionnaire (QOLRAD)
The patient-reported QOLRAD consists of 25 questions combined into a total score ranging from 25 to 175 with higher numbers representing better quality of life.

Full Information

First Posted
June 7, 2006
Last Updated
July 17, 2012
Sponsor
Vanderbilt University
Collaborators
TAP Pharmaceutical Products Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00335283
Brief Title
Efficacy of Lansoprazole in Chronic Post Nasal Drip
Acronym
PND
Official Title
Randomized Placebo-Controlled Trial of BID Lansoprazole in Isolated Chronic Post Nasal Drip
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University
Collaborators
TAP Pharmaceutical Products Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether aggressive acid suppression with Lansoprazole is effective in the treatment of post nasal drip, and also assess the predictors of response based on clinical and physiologic parameters.
Detailed Description
Postnasal drip (PND) is a common complaint that brings patients to the attention of their primary care physicians. It is also one of the most common reasons for patients to seek care from otolaryngologists. Traditionally, PND has been considered and treated as a symptom of sinonasal pathology. It has also been shown, along with Gastroesophageal reflux disease (GERD) and asthma, to be a major contributor to the development of chronic cough. PND refractory to treatment aimed at sinonasal disease is sometimes treated with anti-GERD therapy. This treatment modality is based on clinical experience. To date, there are no studies in the literature to support a causal relationship between PND and extraesophageal reflux (EER). In a case control study of patients with and without esophagitis El-Serag et al reported a significant association (odds ratio 1.6, 95%CI 1.4-1.8) between sinusitis and GERD. A later study by Ulualp et al in 11 CT confirmed cases of chronic sinusitis resistant to therapy with conventional sinus therapies they found a significantly higher prevalence of hypopharyngeal acid exposure in the sinusitis group than controls. Recently, in an open label prospective pilot trial, DiBaise et al treated 11 patients with sinusitis and 19 GERD patients with omeprazole 20mg bid for 3-months. 9/11 sinusitis patients were found to have GERD by pH monitoring and there was moderate (25-89%) improvement in the sinus symptoms in the omeprazole treated group. However, there are currently no placebo-controlled trials assessing efficacy of PPI's in patients with PND.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Larynx Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lansoprazole
Arm Type
Active Comparator
Arm Title
Sugar Pill
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Lansoprazole Tablet
Other Intervention Name(s)
prevacid
Intervention Description
40 mg bid x 16 weeks
Intervention Type
Procedure
Intervention Name(s)
PH and impedence testing
Intervention Description
24 hour ph monitoring
Intervention Type
Procedure
Intervention Name(s)
manometry
Intervention Description
done prior to pH probe to measure length of esophagus
Intervention Type
Drug
Intervention Name(s)
lansoprazole
Intervention Description
40mg bid
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
one tablet bid
Primary Outcome Measure Information:
Title
Post Nasal Drainage Symptom Response
Description
The primary outcome measure was postnasal drainage symptom response measured by using a visual analogue scale. At 8 and 16 weeks, a horizontal symptoms scale from 0% (no change) to 100% (symptoms completely resolved) was presented to participants to assess improvement in postnasal drainage symptoms.
Time Frame
8 and 16 weeks
Secondary Outcome Measure Information:
Title
Rhinosinusitis Outcome Measure(RSOM-31)
Description
RSOM-31 includes 31 questions combined into a total score ranging from 0 to 155 with higher scores representing greater disease burden. Values are based on patient report.
Time Frame
Baseline, 8 weeks, and 16 weeks
Title
Sino Nasal Outcome Test (SNOT-20)
Description
SNOT-20 includes 20 questions combined into a total score ranging from 0 to 100 with higher numbers representing greater rhinosinusitis health burden and represents patient-reported symptom severity.
Time Frame
Baseline, 8 weeks and 16 weeks
Title
Quality of Life Questionnaire (QOLRAD)
Description
The patient-reported QOLRAD consists of 25 questions combined into a total score ranging from 25 to 175 with higher numbers representing better quality of life.
Time Frame
Baseline, 8 weeks and 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael F Vaezi, MD PhD MS
Organizational Affiliation
Vanderbilt University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt University Medical Center, Vanderbilt Digestive Disease Clinic, TVC, Room 1660
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232-5280
Country
United States

12. IPD Sharing Statement

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Efficacy of Lansoprazole in Chronic Post Nasal Drip

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