An 18-week, randomised, double-blind, multicentre, placebo-controlled trial to evaluate the efficacy and safety of rosuvastatin (5 and 10 mg) in the treatment of hypercholesterolaemic postmenopausal women receiving hormone replacement therapy

Study identifier:4522IL/0032

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An 18-week, randomised, double-blind, multicentre, placebo-controlled trial to evaluate the efficacy and safety of rosuvastatin (5 and 10 mg) in the treatment of hypercholesterolaemic postmenopausal women receiving hormone replacement therapy

Medical condition

dyslipidaemia

Phase

Phase 3

Healthy volunteers

-

Study drug

-

Sex

-

Actual Enrollment

-

Study type

Interventional

Age

-

Date

Study Start Date: 01 Jan 1971
Primary Completion Date: -
Study Completion Date: -

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Nov 2013 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria