Barriers to Optimal LDL-C Targets in Patients With Atherosclerotic Cardiovascular Disease
BOLT
Evaluation of Adherence to Cholesterol Therapies and Identification of Barriers to Optimal LDL-C Targets in Patients With Atherosclerotic Cardiovascular Disease
1 other identifier
observational
1,000
1 country
2
Brief Summary
In the present cross-sectional observational study, the investigators aimed to:
- Evaluate the prevalence of achievement of LDL-C targets among a sample of Egyptian ASCVD patients.
- Attempt to unveil the potential barriers to achieve LDL-C goals in order to determine the appropriate corrective actions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2024
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 21, 2024
CompletedFirst Submitted
Initial submission to the registry
March 19, 2025
CompletedFirst Posted
Study publicly available on registry
March 27, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2025
CompletedDecember 3, 2025
December 1, 2025
1.1 years
March 19, 2025
December 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prevalence of achievement of recommended LDL-C targets among patients with established ASCVD
Recruited patients will be stratified according to the LDL-C levels into those \<55, \<70, \<100, \<130, and above. Patients in different LDL-C strata will be surveyed. Predictors for failure of achievement of LDL-C goals will be sought.
Being a cross sectional study selectively recruiting patients with established indication for >6months, the study will accept a fasting lipid profile that was performed within 1 month from surveying the recruited patient.
Interventions
Recruited patients will be requested to provide data from their most recent fasting lipid profile
Eligibility Criteria
Patients with established ASCVD with indication for high-intensity statin for a period 6 months This includes patients with coronary artery disease, peripheral arterial disease, cerebrovascular disease.
You may qualify if:
- Patients presenting to cardiology department/ outpatient clinic.
- Established ASCVD and eligible for high intensity statins for at least six-months.
- Age between18-to-80y.
You may not qualify if:
- Refusal to participate in the survey.
- Recent diagnosis of ASCVD with indication to high intensity statins for a period \< six-months.
- Patients with medical limitation or contraindications to statins therapy.
- Patients with documented diagnosis of homozygous familial hypercholesterolemia.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (2)
Faculty of Medicine Cairo University
Cairo, Egypt
Faculty of Medicine, Cairo University
Cairo, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
March 19, 2025
First Posted
March 27, 2025
Study Start
September 21, 2024
Primary Completion
November 1, 2025
Study Completion
November 1, 2025
Last Updated
December 3, 2025
Record last verified: 2025-12