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The Effect of Nexium on Transmucosal Esophageal Leak

Primary Purpose

Reflux, Esophagitis, Barrett's Esophagus

Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Esomeprazole (Nexium) 40 mg/day
Sponsored by
Main Line Health
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Reflux focused on measuring Sucrose, Barrett's esophagus, Esophagitis, GERD, Reflux, Esophagus, Esomeprazole

Eligibility Criteria

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

Inclusion Criteria: Patients presenting to a general practitioner / internist with symptoms of GERD defined as: Heartburn - uncomfortable, rising, burning sensation behind the breastbone Regurgitation of gastric acid or sour contents into the mouth Chest pain atypical for cardiac ischemia and more suggestive of GERD Symptoms for more than three weeks with no concurrent use of PPI's or H-2 blockers during that time period A score greater than or equal to 5 on the AstraZeneca RDQ Exclusion Criteria: Any patients presenting with alarm symptoms (GI bleeding, dysphagia, weight loss, abdominal mass, lymphadenopathy, or recurrent vomiting) Diabetes (type I or II) Renal insufficiency defined as creatinine >1.6 Under 18 years of age Prior surgery on esophagus, stomach or duodenum History of gastric/duodenal ulcers History of H. pylori Known history of Barrett's esophagus (recruited to parallel study) On Coumadin or Heparin therapy Chronic upper abdominal pain more consistent with dyspepsia or other diagnoses Noncompliant patients

Sites / Locations

  • Lankenau Hospital

Outcomes

Primary Outcome Measures

Urine sucrose level falls below 90 mg after 8 weeks of therapy

Secondary Outcome Measures

Reduction of patient symptoms consistent with GERD

Full Information

First Posted
September 19, 2005
Last Updated
March 15, 2010
Sponsor
Main Line Health
Collaborators
AstraZeneca, Sharpe-Strumia Research Foundation, Cancer Research Foundation of America
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1. Study Identification

Unique Protocol Identification Number
NCT00216788
Brief Title
The Effect of Nexium on Transmucosal Esophageal Leak
Official Title
The Effect of Proton Pump Inhibitors on Transmucosal Esophageal Leak
Study Type
Interventional

2. Study Status

Record Verification Date
November 2005
Overall Recruitment Status
Unknown status
Study Start Date
January 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2006 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Main Line Health
Collaborators
AstraZeneca, Sharpe-Strumia Research Foundation, Cancer Research Foundation of America

4. Oversight

5. Study Description

Brief Summary
In a related study, the investigators have found evidence that patients with Barrett's esophagus have a leak for oral sucrose to leave their upper gastrointestinal tract, enter the blood, and be filtered into urine. The amount of sucrose appearing in an overnight urine sample can be used to indicate the presence of Barrett's esophagus and/or esophagitis in a patient reporting with reflux (GERD) symptoms. The leak is presumably in the Barrett's epithelium itself. This phenomenon will be used to test if a standard 8 week therapy of Nexium in a first-time-presenting GERD patient can reduce the leak as a means of assessing the efficacy of the drug in that patient. The investigators predict that Nexium will reduce leak in esophagitis but not Barrett's patients.
Detailed Description
In a related study, we have found evidence that patients with Barrett's esophagus have a leak for oral sucrose to leave the lumen of their upper gastrointestinal tract, enter the blood, and be filtered into urine. Normally the disaccharide sucrose cannot leave the lumen of the gastrointestinal tract without being first hydrolyzed to glucose and fructose. Appearance of the disaccharide in the bloodstream suggests a paracellular leak of some type in the upper gastrointestinal tract. Once in the blood, sucrose is likewise not taken up or metabolized by the kidney but simply filtered into the urine. The amount of sucrose appearing in an overnight urine sample can be used to indicate the presence of Barrett's esophagus and/or esophagitis in a patient reporting with reflux (GERD) symptoms. The leak is presumably in the Barrett's epithelium itself. This phenomenon will be used to test if a standard 8 week therapy of Nexium in a first-time-presenting GERD patient can reduce the leak as a means of assessing the efficacy of the drug in that patient. We predict that Nexium will reduce leak in esophagitis but not Barrett's patients. In this study, patients over 18 years of age presenting with GERD symptoms to a primary care physician, will be recruited after providing informed consent. Patients will perform a sucrose leak test the evening after their recruitment by drinking a solution of 100 gms of sucrose in 200 cc of water at bedtime, then collecting an overnight urine sample (8 hrs). Within 5 days the patient will undergo an upper endoscopy exam. The patient will then begin Nexium therapy (40 mg/day of Esomeprazole) for 8 weeks, taking the dose each morning before breakfast. After 8 weeks the patient will undergo a second sucrose leak test as described above. Urine sucrose will be determined by HPLC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Reflux, Esophagitis, Barrett's Esophagus
Keywords
Sucrose, Barrett's esophagus, Esophagitis, GERD, Reflux, Esophagus, Esomeprazole

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
35 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Esomeprazole (Nexium) 40 mg/day
Primary Outcome Measure Information:
Title
Urine sucrose level falls below 90 mg after 8 weeks of therapy
Secondary Outcome Measure Information:
Title
Reduction of patient symptoms consistent with GERD

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients presenting to a general practitioner / internist with symptoms of GERD defined as: Heartburn - uncomfortable, rising, burning sensation behind the breastbone Regurgitation of gastric acid or sour contents into the mouth Chest pain atypical for cardiac ischemia and more suggestive of GERD Symptoms for more than three weeks with no concurrent use of PPI's or H-2 blockers during that time period A score greater than or equal to 5 on the AstraZeneca RDQ Exclusion Criteria: Any patients presenting with alarm symptoms (GI bleeding, dysphagia, weight loss, abdominal mass, lymphadenopathy, or recurrent vomiting) Diabetes (type I or II) Renal insufficiency defined as creatinine >1.6 Under 18 years of age Prior surgery on esophagus, stomach or duodenum History of gastric/duodenal ulcers History of H. pylori Known history of Barrett's esophagus (recruited to parallel study) On Coumadin or Heparin therapy Chronic upper abdominal pain more consistent with dyspepsia or other diagnoses Noncompliant patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daniel Lazowick, D.O.
Phone
610-645-6555
First Name & Middle Initial & Last Name or Official Title & Degree
Gambril Murray, M.D.
Phone
610-642-6990
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James M Mullin, Ph.D.
Organizational Affiliation
Main Line Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lankenau Hospital
City
Wynnewood
State/Province
Pennsylvania
ZIP/Postal Code
19096
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daniel Lazowick, D.O.
Phone
610-645-6555
First Name & Middle Initial & Last Name & Degree
Daniel Lazowick, D.O.

12. IPD Sharing Statement

Links:
URL
http://www.pubmed.gov
Description
Related Info

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The Effect of Nexium on Transmucosal Esophageal Leak

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