Condition: Metabolite · Sponsor: National University Hospital, Singapore
This is a 2-arm, prospective, randomized, parallel-group, open-label, longitudinal study that lasts 30 days for each study participant. This study aims to investigate the effect of co-administration of Omeprazole with Atorvastatin versus Atorvastatin monotherapy on atorvastatin lactone level. Primary endpoint: Higher statin lactone level in intervention arm after 30 days. Secondary endpoints: Higher hs-CRP in intervention arm Lipid panel Incidence of adverse drug side effects (e.g. muscle-related or elevated LFTs
This description comes directly from the study's public registry record.
Junietta Lim, Bachelor of Science (Pharmacy) · +65 86136595 · seacolnus@gmail.com
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| National University of Singapore (NUS) MD6 Level 8 | Singapore, Singapore | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06690164