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Registry On Efficacy and Safety Of Rosuvastatin, and Atorvastatin and Simvastatin In Hypercholesterolaemia

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Hypercholesterolaemia

Study type

Observational

Funder types

Industry

Identifiers

NCT01352897
NIS-CSG-CRE-2011/1

Details and patient eligibility

About

The objective of this follow-up retrospective study is to evaluate the long term efficacy and safety of rosuvastatin in reducing lipid parameters in clinical practice.

Enrollment

800 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Primary hypercholesterolemia
  • Subjects from first rosuvastatin Registry study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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