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Centralized Pan-Middle East Survey on the Undertreatment of Hypercholesterolemia

Centralized Pan-Middle East Survey on the Undertreatment of Hypercholesterolemia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01604733
Acronym
CEPHEUS
Enrollment
1000
Registered
2012-05-24
Start date
2010-10-31
Completion date
2011-06-30
Last updated
2012-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypercholesterolemia

Keywords

Multi-Center Survey, patients currently on lipid-lowering pharmacological treatment, level of Control of Hypercholesterolemia in Egypt

Brief summary

Study objective is to evaluate the level of control of hypercholesterolemia in Egypt in patients taking lipid lowering agents for at least 3 months ( with no drug change or dose amendment for a minimum of 6 weeks).

Detailed description

Centralized Pan-Middle East Survey on the Undertreatment of Hypercholesterolemia

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years and above on current lipid lowering drug for at least 3 months with no dose change for a minimum of 6 weeks * Subject must provide informed consent and comply with the survey procedures

Exclusion criteria

* Less than 18 years less than 3 months on antidyslipidemic agent Subjects who are unwilling or unable to provide informed consent

Design outcomes

Primary

MeasureTime frame
The proportion of patients on lipid-lowering treatment reaching the LDL-C goals according to the NCEP ATP III/ updated 2004 NCEP ATP III , overall and by country24 weeks

Secondary

MeasureTime frame
The proportion of patients on lipid-lowering treatment reaching the LDL-C goals according to the NCEP ATP III/ updated 2004 NCEP ATP III , in the following sub-populations: - primary/secondary prevention patients and with metabolic syndromes24 weeks
The proportion of patients on lipid-lowering treatment reaching the LDL-C goals according to the Third Joint European Task Force guideline, in the following sub-populations: - primary/secondary prevention patients and with metabolic syndromes24 weeks
Determinants (e.g. patient and physician characteristics , country-specific guidelines or recommendations) for undertreatment of hypercholesterolemia24 weeks
Physician characteristics associated with the allocation of treatment regimen.24 weeks
The proportion of patients on lipid-lowering treatment reaching the non HDL-C goals according to the NCEP ATP III/ updated 2004 NCEP ATP III , in the sub-population patients with fasting triglycerides<200 mg/d24 weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026