Study identifier:D5040N00006
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Risk of uncomplicated peptic ulcer in the general population
Peptic Ulcer [Iowa Type (107680.0010)]
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No
Risk of symptomatic peptic ulcer
All
4000
Observational
40 Years - 84 Years
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Jul 2014 by AstraZeneca
AstraZeneca
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The analyses are conducted in a previous population-based cohort study using The Health Improvement Network database in the UK (Cai et al 2009).The aims of the post hoc analyses are: To estimate the relative risk of uncomplicated symptomatic peptic ulcer (UPU) associated with use of low dose aspirin (ASA) and other anti-inflammatory drugs (NSAIDs, steroids) in the general population To estimate the dose-response and duration-response associated with use of these drugs To estimate the relative risk of UPU associated with naive/non-naive use of low dose ASA in the general population To evaluate the effect of proton pump inhibitors (PPI) (alone or in combination with anti-inflammatory drugs) on the occurrence of UPU in the general population To investigate the management of low dose ASA/oral antiplatelets after UPU
Risk of uncomplicated peptic ulcer in the general population
Location
Location
Madrid, Spain
Arms | Assigned Interventions |
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Cases Patients with symptomatic peptic ulcer (UPU) | Drug: Risk of symptomatic peptic ulcer Current use of drugs (ASA; NSAIDs, SSRI,PPI, H2RA) versus non-use |
Control group Control group without symptomatic peptic ulcer (UPU). | Drug: Risk of symptomatic peptic ulcer Current use of drugs (ASA; NSAIDs, SSRI,PPI, H2RA) versus non-use |
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