Reduction Efficacy of OLOMAX for Blood Pressure and Low-density Lipoprotein Cholesterol in Hypertensive Patients With Dyslipidemia

Last updated: January 21, 2025
Sponsor: Daewoong Pharmaceutical Co. LTD.
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Circulation Disorders

Williams Syndrome

Stress

Treatment

Olmesartan Medoxomil/ Amlodipine Besylate/ Rosuvastatin Ca

Clinical Study ID

NCT05660135
DWOLM_RWE02
  • Ages > 19
  • All Genders

Study Summary

This study is a large-scale, prospective, multi-center, and non-interventional observation study to observe blood pressure and blood lipid changes and safety during administration of olomax tablets for 24 weeks in hypertensive patients with dyslipidemia.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Adult aged 19 or older at the time of the baseline visit.

  2. A patient with hypertension and dyslipidemia who is scheduled to administer olomaxtablet according to investigator's medical judgement.

  • Patients who were previously taking more than two tablets of a single drug,low-density lipoprotein-cholesterol (LDL-C)

  • Patients who were previously only taking blood pressure-lowering drugs and didnot take LDL-C-lowering drugs, but who need to take additional LDL-C-loweringdrugs at the discretion of the researcher

  • Patients who were previously taking LDL-C lowering agents and did not takeblood pressure lowering agents, but who need to take additional blood pressurelowering agents according to the researcher's judgment

  • Patients who have not previously taken both a blood pressure drop and an LDL-Cdrop but need additional simultaneous use at the discretion of the researcher

  1. A person who can understand the information provided to him/her and may voluntarilysign a written consent form

Exclusion

Exclusion Criteria:

  1. A person who falls under the prohibition of administration according to thepermission for olomax tablet

  2. A person who has a history of administering olomax tablets before participating inthis study

  3. In addition to the above, a person that the investigator thinks he/she is notsuitable for participating in this observation study;

Study Design

Total Participants: 4000
Treatment Group(s): 1
Primary Treatment: Olmesartan Medoxomil/ Amlodipine Besylate/ Rosuvastatin Ca
Phase:
Study Start date:
June 20, 2022
Estimated Completion Date:
June 30, 2025

Study Description

In this study, investigator will evaluate subjects' clinical performance in actual care. Laboratory test results such as demographic information and medical treatment, blood pressure, blood lipid test, and liver function test conducted at the start date of Olomax tablet administration and subsequent 24 weeks (± 8 weeks) will be collected. In the case of safety-related information, such as abnormal cases, data shall be collected at any time during the 24-week follow-up period if there is a visit by the study subject according to daily treatment.

Connect with a study center

  • Seoul St.Mary's Hospital

    Seoul,
    Korea, Republic of

    Active - Recruiting

  • The Catholic University of Korea, Seoul ST. Mary's Hospital

    Seoul,
    Korea, Republic of

    Site Not Available

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