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Dietary Intervention to Stop COronary Atherosclerosis in Computed Tomography

Not Applicable
Conditions
Coronary Artery Disease
Registration Number
NCT02571803
Lead Sponsor
National Institute of Cardiology, Warsaw, Poland
Brief Summary

The aim of the study is to determine, wheather strict dietary intervention with the use of the DASH diet atop of optimal medical treatment reduces previously diagnosed coronary atherosclerotic lesions assessed witch coronary computed tomography.

Detailed Description

A total of 180 patients with coronary atheroslerotc lesions confirmed in coronary computed tomography (CCT) will be analyzed in a 12-month observation time. Patients will be randomized to two groups in a 1:1 fashion. 1 - optimal medical treatment, 2 - strict dietary intervention with implementation of the DASH diet atop of optimal medical treatment. CCT scans will be performed at screening and at 12 months after randomization. Computed tomography imaging data describing atheroslerotic lesions will be assessed.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
180
Inclusion Criteria
  • coronary atheroslerotic lesions confirmed in the screening CCTA with reduction of the artery diameter less than 70% in 2 or more coronary artery segments
  • no indications for coronary angiography / revascularization (no documented significant ischemia of myocardium)
  • free and informed consent of the person concerned
  • willingness to follow the strict directions given by the investigators
Exclusion Criteria
  • any valvular heart disease requiring cardiac surgery (or expected cardiac surgery intervention within 12 moths)
  • diagnosis of dilated / hypertrophic cardiomyopathy
  • diagnosis of DM t. 2
  • past CABG procedure
  • women in reproductive age
  • known genetic factors with a possible impact on the progres of coronary atherosclerotic lesions (e. i. congenital metabolic disorders, familial hyperlipidemias)
  • low quality of the CCTA data

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Percent Of Patheroma Volume (PAV)12 months

Reduction of percent atheroma volume (PAV) measured between baseline and follow-up CT scans.

Secondary Outcome Measures
NameTimeMethod
Pericardial Fat Distribution12 months

Change in pericardial fat distribution between baseline and follow-up CT scans.

Trial Locations

Locations (1)

Institute of Cardiology

🇵🇱

Warsaw, Poland

Institute of Cardiology
🇵🇱Warsaw, Poland
Jan Henzel, MD
Contact
+48223434342
jhenzel@ikard.pl
Cezary Kepka, prof.
Contact
+48223434342
ckepka@ikard.pl

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