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A study to monitor the safety profile of statins in participants

Safety profile of statins in patients at a tertiary care center- A prospective study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/06/069448
Enrollment
288
Registered
2024-06-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: NIL: Nil Control Intervention1: NIL: Nil

Sponsors

Dr Yash Goel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients (aged 18 years or older) of any gender or ethnicity. Patients requiring statin therapy. Patients who are willing and able to provide informed consent.

Exclusion criteria

Exclusion criteria: Patients with severe liver or kidney dysfunction Patients with uncontrolled malignancy or other life-threatening conditions. Pregnant or breastfeeding women. Patients with uncontrolled endocrine disorders Patients with cognitive impairment or psychiatric disorders that may interfere with their ability to provide informed consent or comply with the study protocol. patients who are unwilling to give consent

Design outcomes

Primary

MeasureTime frame
To Study the safety profile of statin therapy at a tertiary care centre Timepoint: To Study the safety profile of statin therapy at a tertiary care centre at every 4 weeks

Secondary

MeasureTime frame
To evaluate the adverse effects associated with the use of statins. Timepoint: To evaluate the adverse effects associated with the use of statins at every 4 weeks

Countries

India

Contacts

Public ContactDr Yash Goel

Teerthanker Mahaveer University Medical College and Research Centre

drpsmatreja@yahoo.co.in9855001847

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026