premalignant gastric lesions
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patients undergoing a surveillance endoscopy because of a previous diagnosis of intestinal metaplasia or dysplasia of the gastric mucosa Patients with gastric intestinal metaplasia or dysplasie diagnosed after the start of the study
Exclusion criteria
Exclusion criteria: Coagulopathy uncorrected at the time of endoscopy or thrombocytopenia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of detected lesions with histological proven intestinal metaplasia or dysplasia after NBI-ME as compared to the number of detected lesion with histological proven intestinal metaplasia or dysplasia after conventional endoscopy. | — |
Secondary
| Measure | Time frame |
|---|---|
| Correspondence between serologic markers (pepsinogen I, II and gastrin 17) and H. pylori data and histology | — |
Countries
Netherlands
Outcome results
None listed