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An observational Study on the post-Acute coronary syndrome Patients with uncontrolled hyperlipidemia in China

An observational Study on the post-Acute coronary syndrome Patients with uncontrolled hyperlipidemia in China

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15005982
Enrollment
Unknown
Registered
2015-02-14
Start date
2015-03-22
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hyperlipidemia

Interventions

ACS subjects with uncontrolled Hyperlipidemia:NA

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who have experienced an ACS event within the past 4-40 weeks. ACS event including - hospitalization for ACS (ST-elevation MI, non-ST elevation MI or high-risk unstable angina); 2. Patients receiving active lipid lowering treatment with a stable (>2 weeks) regimen; 3. Patients' lipid level not tested after stable active lipid lowering treatment or tested but not adequately controlled indicated by a lipid test after stable active lipid lowering treatment; 4. At least 40 years of age; 5. Patient having provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. Unable or unwilling to provide informed consent, including but not limited to cognitive or language barriers to comprehension; 2. Participation in any clinical trial at the time of enrollment; 3. Life expectancy <1 year.

Design outcomes

Primary

MeasureTime frame
Percentage of patients who have experienced an ACS event within the past 4-40 weeks and not achieving their respective therapeutic goal undertaking statin-intensive treatment.;Percentage of patients who have experienced an ACS event within the past 4-40 weeks and not achieving their respective therapeutic goal undertaking maximally tolerated dose of these given statins and other non-statin lipid lowering therapy if patient has documented intolerance to at least 2 statins at physician’s discretion in China.;

Secondary

MeasureTime frame
Medical reasons that limit the adoption of intensive statin treatment when patient’s therapeutic goal is not achieved.;

Countries

China

Contacts

Public ContactXu CAO
bonnie.cao@sanofi.com+86 10 65634983

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026