Skip to content

Dyslipidemia management in patients with the first acute coronary event: A real world study based on electronic medical records

Dyslipidemia management in patients with the first acute coronary event: A retrospective observational EMR based RWE study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/07/043875
Enrollment
470
Registered
2022-07-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: E785- Hyperlipidemia, unspecified

Interventions

Intervention1: Nil: Nil

Sponsors

Dr Reddys Laboratories Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Electronic medical data of Patients with a confirmed diagnosis (either by angiography or clinical findings) of the first ACS event (STEMI [ST elevation myocardial infarction]/NSTEMI [non-ST elevation myocardial infarction]/ unstable angina) 2 Minimum of 12 months of follow-up data post statin therapy initiation 3 Patients initiated statin therapy prior to or post first ACS event 4 Patients considered for initiation/ maintenance/ modification of statin therapy before discharge from hospital

Exclusion criteria

Exclusion criteria: EMR of Patients with a history of hospital admission for ACS in the past 12 months before the index event , type 1 diabetes mellitus, history of malignancy, patients with active or suspected or with history of hepatic or stage 5 renal disease, history of uncontrolled hypothyroidism, alcohol, or drug abuse, Patients on hormone replacement therapy or oral contraceptives within 3 months of enrollment or pregnant patient

Design outcomes

Primary

MeasureTime frame
1 The dose of statin/statin plus other lipid-lowering therapies after the first ACS event at discharge and the end of 12 months 2 The proportion of patients with a history of dyslipidemia and first ACS event and the dose of statins/statin plus other lipid-lowering therapies during/before the event, at discharge and the end of 12 monthsTimepoint: Baseline and 12 months

Secondary

MeasureTime frame
1 percentage of patients with co-morbid conditions and risk factors stratified by age and sex 2 Utilization pattern of statin/statin plus other lipid-lowering therapy in dyslipidemia patients with first ACS event and having comorbidities 3 Incidence rates of recurrent ACS, stroke, heart failure, revascularization, and cardiovascular-specific deaths reportedTimepoint: Baseline or discharge from hospital and end of 12 months

Countries

India

Contacts

Public ContactDr Rahul Rathod

Dr Reddys Laboratories ltd

rahul.rathod@drreddys.com

Outcome results

None listed

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