Viewing Study NCT06379295


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Ignite Modification Date: 2026-02-21 @ 1:51 AM
Study NCT ID: NCT06379295
Status: COMPLETED
Last Update Posted: 2024-11-01
First Post: 2024-04-18
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Coronary Artery Calcification Assessed on PET Scanner (PET : Positron Emission Tomography)
Sponsor: Centre Hospitalier Régional d'Orléans
Organization:

Study Overview

Official Title: Coronary Artery Calcification Assessed on PET Scanner (PET : Positron Emission Tomography)
Status: COMPLETED
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CALCOTEP
Brief Summary: Calcification artery calcium (CAC) scoring is a valuable tool for determining the risk of major adverse cardiac events.

It was found that CAC can be quantitatively assessed, by manual scoring or using deep-learning, on low-dose non electrocardiogram-gated, contrast-enhanced or non-enhanced computed tomography (CT-scan) performed in association of PET acquisition, with a good agreement with standard scans.

The purpose of this study is to determine the impact of a systematic coronary artery calcification evaluation in patients undergoing flourine-18 fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) imaging to improve primary prevention of cardiovascular diseases.

A visual calcification artery calcium assessment will be made for each patient, dividing them into four groups: none, mild, moderate or heavy calcification artery calcium. When possible, a calcification artery calcium score will be computed.

Each patient will complete a questionnaire to collect risk factors, history of cardiovascular diseases and medications.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: