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Clinical Trial Summary

The purpose of this study is to investigate whether bariatric surgery affects Drospirenone only pills absorption


Clinical Trial Description

After being informed about the study and potential risks, all participants giving written informed consent who meet the eligibility requirements will take Drospirenone-only pills (4 mg, once daily). Between the 21st and 28th day of Drospirenone taking, pharmacokinetics will be measured. Pre-bariatric surgery pharmacokinetics study will be compared with post-bariatric surgery pharmacokinetics study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06345560
Study type Interventional
Source Chulalongkorn University
Contact Punyawee Utaipatanacheep
Phone +668-7515-4003
Email punyawee@docchula.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date April 2024
Completion date April 2025

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