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NCT05411887Active, not recruiting

Study to Evaluate the Effect of Improving Systolic BP and LDL-C Compared to Conventional Treatments and the Convenience of Taking Medication of Olostar Tab

A Non-interventional, Multi Center, Prospective Observational Study to Evaluate the Effect of Improving Systolic Blood Pressure and Low-density Lipoprotein Cholesterol Compared to Conventional Treatments and the Convenience of Taking Medication of Olostar Tab. in Patients With Essential Hypertension and Dyslipidemia.

Source: ClinicalTrials.gov · Last updated 24 Aug 2025

Brief summary (registry, in English)

The purpose of this study is to evaluate the effectiveness of Olostar Tablet on blood pressure and lipid profiles, obtain safety-related information for subgroups that failed to participate in the clinical trials, and to evaluate variables that affect treatment effectiveness.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
2845 (actual)
First submitted
19 May 2022
Start date
20 Jun 2022
Primary completion date
31 Mar 2025
Lead sponsor
Daewoong Pharmaceutical Co. LTD.
NCT number
NCT05411887

What you commit to

  • Study type: Observational
  • Participants enrolled: 2845
  • From 20 Jun 2022 to the primary completion date, 31 Mar 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • A person who has been administered the study target drug or is being administered at the time of recruitment within 6 months based on the date of the study contract

Other

  • A person who falls under "2. Do not administer to the following patients" among the precautions for use in the user manual
  • Patients in hospital (hospitals only; nursing care facilities can be recruited)

Who the study is looking for

  • men and women over the age of 19
  • Patients who signed a written consent form to participate in the study
  • Patients who are eligible for Olostar tablet prescription according to domestic permission

Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Severance hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.