Esomeprazole Treatment for Patients With Lymphocytic Gastritis (LYNEX)
Primary Purpose
Lymphocytic Gastritis
Status
Unknown status
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Esomeprazole
Sponsored by
About this trial
This is an interventional treatment trial for Lymphocytic Gastritis
Eligibility Criteria
Inclusion Criteria:
- Histologically proven lymphocytic gastritis (IEL > 25/100)
- Male or female aged 18 years or older
- Signed and written informed consent
Exclusion Criteria:
- Regular NSAID or aspirin intake
- Concomitant medication with antibiotics, bismuth subsalicylate, aminosalicylates
- Regular PPI therapy
- Treatment with ketoconazole or other CYP3A inhibitors
- previous surgery of the stomach
- known or suspected hypersensitivity to esomeprazole
- Malignant diseases
- Concomitant severe diseases
- Pregnancy or lactation
- Contraindication to take biopsies (Quick < 50%, PTT > 50 s, thrombocytes < 100.000/mm3)
Sites / Locations
- Medical Department I, University Hospital Carl Gustav Carus, Technical UniversityRecruiting
Outcomes
Primary Outcome Measures
The primary objective is to assess the healing rate of
patients with lymphocytic gastritis irrespective of H. pylori status after treatment
with esomeprazole 20 mg twice daily for 2 weeks.
Secondary Outcome Measures
Secondary objective of the study are to evaluate the grade and activity of gastritis before and after
treatment according to updated Sydney classification, to assess the clinical GI symptoms at baseline and after 3 months
and to evaluate influence of the H. pylori-Status
Full Information
NCT ID
NCT00455754
First Posted
April 3, 2007
Last Updated
April 3, 2007
Sponsor
Technische Universität Dresden
1. Study Identification
Unique Protocol Identification Number
NCT00455754
Brief Title
Esomeprazole Treatment for Patients With Lymphocytic Gastritis
Acronym
LYNEX
Official Title
Double-Blind, Randomized, Placebo-Controlled Multicenter Trial on the Efficacy of Esomeprazole Treatment for Patients With Lymphocytic Gastritis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2007
Overall Recruitment Status
Unknown status
Study Start Date
February 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2009 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Technische Universität Dresden
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether treatment with esomeprazole alone is able to heal patients with lymphocytic gastritis
Detailed Description
Recently, a placebo controlled trial of our group has shown that H. pylori eradication therapy consisting of omeprazole 20 mg bid, clarithromycin 500 mg bid, amoxicillin 1000 mg bid for seven days leads to a complete long-lasting resolution of lymphocytic gastritis in 96 % of patients. However, after 3 months we also found a healing rate of 50 % in patients who received omeprazole 20 mg bid and placebo antibiotics for seven days suggesting spontaneous remission or a potential PPI effect. Thus, we speculate that PPI therapy may have led to elimination of H. pylori and subsequently healing of lymphocytic gastritis in those patients with potentially minimal H. pylori colonization at baseline. For this reason we investigate whether a PPI treatment alone is able to heal patients with lymphocytic gastritis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphocytic Gastritis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
40 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Esomeprazole
Primary Outcome Measure Information:
Title
The primary objective is to assess the healing rate of
Title
patients with lymphocytic gastritis irrespective of H. pylori status after treatment
Title
with esomeprazole 20 mg twice daily for 2 weeks.
Secondary Outcome Measure Information:
Title
Secondary objective of the study are to evaluate the grade and activity of gastritis before and after
Title
treatment according to updated Sydney classification, to assess the clinical GI symptoms at baseline and after 3 months
Title
and to evaluate influence of the H. pylori-Status
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically proven lymphocytic gastritis (IEL > 25/100)
Male or female aged 18 years or older
Signed and written informed consent
Exclusion Criteria:
Regular NSAID or aspirin intake
Concomitant medication with antibiotics, bismuth subsalicylate, aminosalicylates
Regular PPI therapy
Treatment with ketoconazole or other CYP3A inhibitors
previous surgery of the stomach
known or suspected hypersensitivity to esomeprazole
Malignant diseases
Concomitant severe diseases
Pregnancy or lactation
Contraindication to take biopsies (Quick < 50%, PTT > 50 s, thrombocytes < 100.000/mm3)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmed Madisch, MD
Phone
++493514584780
Email
ahmed.madisch@uniklinikum-dresden.de
First Name & Middle Initial & Last Name or Official Title & Degree
Stephan Miehlke, Prof., MD
Phone
++493514585645
Email
stephan.miehlke@uniklinikum-dresden.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed Madisch, MD
Organizational Affiliation
Medical Department I, University Hospital Carl Gustav Carus, Technical University Dresden, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical Department I, University Hospital Carl Gustav Carus, Technical University
City
Dresden
ZIP/Postal Code
01307
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ahmed Madisch, MD
Phone
++493514584780
Email
ahmed.madisch@uniklinikum-dresden.de
First Name & Middle Initial & Last Name & Degree
Stephan Miehlke, Prof.
Phone
++493514585645
Email
stephan.miehlke@uniklinikum-dresden.de
12. IPD Sharing Statement
Learn more about this trial
Esomeprazole Treatment for Patients With Lymphocytic Gastritis
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