An Observational Study Investigating the Change in Blood Cholesterol With Mevalotin® Tablet Admin… (NCT05120895) | Clinical Trial Compass
CompletedNot Applicable
An Observational Study Investigating the Change in Blood Cholesterol With Mevalotin® Tablet Administration in Korean Menopausal Women Aged 50 Years or More Who Require Treatment of Dyslipidemia
South Korea3,060 participantsStarted 2021-08-10
Plain-language summary
This study will investigate the efficacy and safety based on the observation of the blood cholesterol change with Mevalotin® Tablet administration in Korean menopausal women aged 50 years or more who require treatment of dyslipidemia.
Who can participate
Age range50 Years
SexALL
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Inclusion Criteria:
* Menopausal women aged 50 years or more diagnosed with dyslipidemia
* Menopause was defined as the condition of not having menstruation for 1 year with no specific cause or being diagnosed with menopause at the discretion of an investigator (except for the case of being diagnosed with menopause for a surgical reason within 5 years), and the menopausal status is confirmed as of the Mevalotin® Tablet administration start date (Index date).
* Patients who are determined to be prescribed with Mevalotin® Tablet at the discretion of an investigator or patients who started Mevalotin® Tablet administration within 6 weeks prior to enrollment in this observational study (however, in case of patients switching from statins to Mevalotin® Tablet, only those who receive from low/intermediate intensity statins treatment to low/intermediate intensity statins treatment can be enrolled in this study)
* Patients who provided voluntary written consent to take part in this observational study
Exclusion Criteria:
* Patients with a history of cancer within 5 years (however, patients with a history of brain tumor, breast cancer, uterine cancer, ovarian cancer, or endometrial cancer are excluded from enrollment regardless of duration.)
* Patients who received hormone replacement therapy within 1 year of enrollment
* Patients who are determined to be ineligible for participation in this observational study
What they're measuring
1
Change from baseline in low-density lipoprotein cholesterol at Week 24 after Mevalotin® Tablet administration