Status:

COMPLETED

Study to Evaluate the Safety of the Fixed-dose Combination Rosuvastatin/Ezetimibe for Patients With Dyslipidaemia

Lead Sponsor:

Laboratorios Silanes S.A. de C.V.

Conditions:

Dyslipidemias

Eligibility:

All Genders

18+ years

Brief Summary

Retrospective, analytical, longitudinal, multicenter study to evaluate the safety of the fixed-dose combination of rosuvastatin / ezetimibe as treatment for patients with dyslipidemia in routine medic...

Detailed Description

To assess the safety of the fixed-dose combination of rosuvastatin / ezetimibe in subjects older than 18 years of age (gender indistinct) with dyslipidemia who at the discretion have been candidates f...

Eligibility Criteria

Inclusion

  • Age\> 18 years of age.
  • Diagnosis of dyslipidemia.
  • That treatment with the fixed-dose combination of rosuvastatin / ezetimibe is documented.
  • Have security questioning on at least two occasions.

Exclusion

  • Subjects who has taken any other statins, fibrates, bile acid sequestrants, niacin (\> 500 mg) or inhibitors of PCSK9 concomitantly during treatment with rosuvastatin / ezetimibe.

Key Trial Info

Start Date :

September 30 2021

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

February 15 2022

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT04862962

Start Date

September 30 2021

End Date

February 15 2022

Last Update

March 2 2022

Active Locations (1)

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Laboratorio Silanes, S.A. de C.V.

Mexico City, Mexico, 11000