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Prospective observational study to investigate lipid-related residual risks for the patients with acute coronary syndrome who were administrated high-dose strong statin

Prospective observational study to investigate lipid-related residual risks for the patients with acute coronary syndrome who were administrated high-dose strong statin - Investigation of lipid-related residual risks after acute coronary syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051955
Enrollment
80
Registered
2023-08-20
Start date
2021-04-13
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute myocardial infarction

Interventions

Rosuvastatin 10md/day

Sponsors

Iwate Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who diagnosed as AMI based on 4th universal definition and underwent percutaneous coronary intervention

Exclusion criteria

Exclusion criteria: (1) Cases who have a contraindication of rosuvastatin treatment (such as in patients receiving cyclosporine) or requires cautious administration (patients with hypothyroidism or patients planning to use fibrates other than fenofibrate). (2) Cases who have a side effects like muscle pain and poor tolerability to rosuvastatin oral administration. (3) Cases who have already used or have a plan to use other high cholesterol-improving medications (such as evolocumab or ezetimibe) during the observation period. (4) Cases of familial hypercholesterolemia. (5) Cases with chronic inflammatory diseases (autoimmune diseases) or ongoing cancer treatment. (6) Cases with impaired consciousness, general malaise, or severe mental disorders. (7) Other cases who are deemed inappropriate by the investigator.

Design outcomes

Primary

MeasureTime frame
The patients who fully achieved the guideline-recommended goal of lipid management, were defined as "achieved group". All the rest were defined as "unachieved group". Of them, incidence and relative factor of the unachieved group will be assessed in the present study.

Countries

Japan

Contacts

Public ContactMasaru Ishida

Iwate Medical University Department of Internal Medicine, Division of Cardiology

maishida@iwate-med.ac.jp019-613-7111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026