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Lipid-lowering Therapy for Secondary Prevention in Patients Undergoing Elective Percutaneous Coronary Intervention (PCI)

AstraZeneca logo

AstraZeneca

Status

Terminated

Conditions

Coronary Artery Disease

Study type

Observational

Funder types

Industry

Identifiers

NCT01190072
NIS-CSI-DUM-2010/1

Details and patient eligibility

About

The purpose of the study is to follow the management of blood lipids in patients with planned percutaneous coronary intervention (widening of coronary vessels) in a period from 6 to 10 weeks after the intervention.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or nonpregnant female
  • Coronary patient hospitalised for elective PCI
  • Hypercholesterolaemia defined as LDL-C ≥ 2 mmol/L

Exclusion criteria

  • Any chronic inflammatory condition
  • Chronic anti-inflammatory pharmacotherapy (except low-dose ASA)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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