The Effect of Nexium on Transmucosal Esophageal Leak
Information source: Lankenau Institute for Medical Research
Information obtained from ClinicalTrials.gov on October 19, 2009 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Reflux; Esophagitis; Barrett's Esophagus
Intervention: Esomeprazole (Nexium) 40 mg/day (Drug)
Phase: Phase 1
Status: Not yet recruiting
Sponsored by: Lankenau Institute for Medical Research Official(s) and/or principal investigator(s): James M Mullin, Ph.D., Principal Investigator, Affiliation: Lankenau Institute for Medical Research
Overall contact: Daniel Lazowick, D.O., Phone: 610-645-6555
Summary
In a related study, we 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. We predict that Nexium will reduce leak in esophagitis but not
Barrett's patients.
Clinical Details
Official title: The Effect of Proton Pump Inhibitors on Transmucosal Esophageal Leak
Study design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study
Primary outcome: Urine sucrose level falls below 90 mg after 8 weeks of therapy
Secondary outcome: Reduction of patient symptoms consistent with GERD
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.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
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
Locations and Contacts
Daniel Lazowick, D.O., Phone: 610-645-6555
Lankenau Hospital, Wynnewood, Pennsylvania 19096, United States
Additional Information
Starting date: January 2006
Ending date: January 2006
Last updated: November 14, 2005
|