Status:
COMPLETED
Retrospective Survey Evaluating the Effectiveness and Safety of Dual Inhibition Lipid-lowering in the Treatment of Dyslipidemia (Study P05171)(COMPLETED)
Lead Sponsor:
Organon and Co
Conditions:
Dyslipidemia
Eligibility:
All Genders
20-75 years
Brief Summary
This retrospective study evaluates the effectiveness and safety of ezetimibe plus statin or ezetimibe plus fenofibrate in dyslipidemic patients that were treated with these dual inhibition lipid lower...
Detailed Description
Retrospective medical chart review
Eligibility Criteria
Inclusion
- Patient was \> 20 years and \< 75 years of age on the index date\*
- Patient diagnosed with dyslipidemia who did not respond adequately based on NCEP ATP III target to previous lipid lowering treatment, and have received dual inhibition therapy, such as ezetimibe plus statins, ezetimibe plus fenofibrate or ezetimibe alone, for at least 3 months
- Patient has at least one Total Cholesterol and LDL-C measurements at baseline and 3 months after initiating the dual inhibition therapy.
- Patient has the following records documented in the chart during the data collection period:
- Medical history and co morbidities (if available)
- Total Cholesterol and LDL-C. test results before and after initiating the dual inhibition therapy
- Prescription information of lipid-lowering dual inhibition regimens NOTE: \* Index date: the date of initiating dual inhibition therapy
Exclusion
- Patients who do not meet all the inclusion criteria will be excluded from this survey.
- Patients who were enrolled in other clinical trial observing specific study procedures which deviates from normal practice will not be included in this study.
Key Trial Info
Start Date :
May 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
July 1 2007
Estimated Enrollment :
1200 Patients enrolled
Trial Details
Trial ID
NCT00726856
Start Date
May 1 2007
End Date
July 1 2007
Last Update
February 16 2022
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