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Effects of high- versus LOw-intensity lipid-lowering treatment in patients undergoing serial CoronAry compuTEd tomography angiography:Results of the multi-center LOCATE study

Conditions
I25
Chronic ischaemic heart disease
Registration Number
DRKS00031954
Lead Sponsor
GRN-Klinikum Weinheim
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
216
Inclusion Criteria

Availability of images from at least 64-slice cardio-CT scanner.
Documentation of lipid-lowering therapy at time of serial cardio-CT scan.

Exclusion Criteria

Pregnancy/Lactation.
Patients without atherosclerotic lesions at baseline and follow-up.
Patients undergoing PCI or CABG between the 2 CCTA scans.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serial quantitative evaluation of plaque size and composition in patients with no/low versus moderate/high dose lipid-lowering therapy.
Secondary Outcome Measures
NameTimeMethod
Verification of results by analysis of inter- and intraobserver (>4 weeks) variability.
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