Evaluation of the Functional Impact of Coronary Stenoses in Diabetics by Spectral CT

NCT ID: NCT05471687

Last Updated: 2022-07-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2025-03-01

Brief Summary

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The optimal screening methods for coronary insufficiency, a frequent and pejorative complication in diabetics, are subject to debate, particularly in situations of silent myocardial ischemia. The contemporary strategy consists of pre-selecting asymptomatic patients at very high cardiovascular (CV) risk by performing a coronary calcium score. If this is found to be high \>300 AU (Agatston units), the patient is suspected of being at high risk of silent myocardial ischemia (SMI), and the assessment is completed to exclude the presence of coronary artery disease likely to benefit from revascularization.

The complementary evaluation consists in evaluating the myocardial perfusion to judge the perfusion repercussions. The most common examination to date is myocardial scintigraphy, because stress tests are too frequently submaximal in diabetics. However, the reproducibility of scintigraphy is controversial and their sensitivity and specificity are debated in this indication.

This problem is similar in stable symptomatic coronary diabetic patients for whom an indication for functional examinations is justified.

The double-energy double-layer spectral scanner (SDEDC) could now become a relevant tool in this field, since it can combine not only anatomical data (identification of coronary stenosis) but also functional data (myocardial perfusion) during a stress protocol. thanks to the spectral images which make it possible to measure the tissue concentration of intramyocardial iodine downstream of the considered stenosis.

Detailed Description

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Conditions

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Coronary Stenosis Diabetic

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Patients with CAC ≥ 300 three years ago

Patients with CAC ≥ 300 three years ago with the need for repeat screening. Adult asymptomatic diabetic patients whose risk of ischemic complications is considered major in primary prevention due to a calcium score \>300 AU and requiring iterative screening for IMS recommended every 3 at 5 years.

Group Type EXPERIMENTAL

dual-energy dual-layer spectral scanner

Intervention Type DEVICE

Realization of dual-energy dual-layer spectral scanner with stress protocol

Stress protocol with adenosin during dual-energy dual-layer spectral scanner

Intervention Type DRUG

Injection of intraveinous adenosin dose 0.78 mg/kg during dual-energy dual-layer spectral scanner

Patients with CAC between 200-299 three years ago

Patients with CAC between 200 and 299 three years ago, with the need for a reassessment of their cardiovascular risk.

Adult asymptomatic diabetic patients whose risk of ischemic complications is considered major in primary prevention due to a calcium score that has become pathological \> 300 AU during the reassessment of their cardiovascular risk.

Group Type EXPERIMENTAL

dual-energy dual-layer spectral scanner

Intervention Type DEVICE

Realization of dual-energy dual-layer spectral scanner with stress protocol

Stress protocol with adenosin during dual-energy dual-layer spectral scanner

Intervention Type DRUG

Injection of intraveinous adenosin dose 0.78 mg/kg during dual-energy dual-layer spectral scanner

Patients with a recent positive scintigraphy (< three months)

Patients with a recent positive scintigraphy (\< three months) requiring coronary angiography Stable symptomatic diabetic adult patients, suspected of coronary insufficiency in whom the assessment included a positive scintigraphy with indication of coronary angiography in the perspective of revascularization.

Group Type EXPERIMENTAL

dual-energy dual-layer spectral scanner

Intervention Type DEVICE

Realization of dual-energy dual-layer spectral scanner with stress protocol

Stress protocol with adenosin during dual-energy dual-layer spectral scanner

Intervention Type DRUG

Injection of intraveinous adenosin dose 0.78 mg/kg during dual-energy dual-layer spectral scanner

Interventions

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dual-energy dual-layer spectral scanner

Realization of dual-energy dual-layer spectral scanner with stress protocol

Intervention Type DEVICE

Stress protocol with adenosin during dual-energy dual-layer spectral scanner

Injection of intraveinous adenosin dose 0.78 mg/kg during dual-energy dual-layer spectral scanner

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Aged man ≥50 years old or woman aged ≥55 years old, (age difference justified for established menopause which increases the CV risk and to avoid the risk of CT scan during pregnancy)
* Diabetic (type 1 or type 2 or type 3):
* Asymptomatic, falling within the scope of screening for silent myocardial ischemia and having a CAC \> 300 AU or
* Symptomatic on the coronary level, within the framework of the evaluation of symptomatic coronary insufficiency with positive myocardial scintigraphy.
* Patient having agreed to participate in the study and signed a written informed consent
* Patient affiliated to a social security scheme or similar

Exclusion Criteria

Drug intolerance (adenosine, and/or contrast product used (Iomeron))

Related to iodine injection:

* History of major immediate or delayed skin reaction + hypersensitivity to the active substance or to any of the excipients
* Renal failure with GFR \< 45 ml/min -
* Known autonomic goiter with risk of thyrotoxicosis
* No suspension of the biguanide the same day of the examination (and resumed 48 hours later)

Linked to the injection of adenosine and regadenoson (Cf SPC Adenoscan combination with dipyridamole)

* 2nd or 3rd degree BAV not fitted, sinus dysfunction not fitted,
* Long QT syndrome,
* Decompensated heart failure,
* Unstable angina / Acute coronary syndrome / ATCD IDM less than a year old
* BP \> 1800 mmHg \< 100 mmHg
* Known stenosis of the common trunk (left),
* Tight heart valve stenosis.
* Uncorrected hypovolemia,
* Chronic obstructive pulmonary disease with clinical bronchospasm (e.g. bronchial asthma)
* Comitiality
* No suspension of dipyridamole (during the 48 hours before the examination)
* Severe hypotension
* Consumption of coffee, tobacco, tea, cola, banana, chocolate consumed before the examination (usual instructions in the event of myocardial stress protocol by adenosine agonist during the scintigraphy)
* Contraindication to adenosine: severe hypotension

Related to scanner performance

* patient unable to maintain apnea.
* Calcium score \> 500 on the common trunk
* Temporary suspension of bradycardia or anti-anginal on the day of the examination (beta blocker, calcium channel blocker) not carried out.

Related to the patient's context

* Person unable to express their consent.
* Patient under guardianship, curatorship or safeguard of justice
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hospices Civils de Lyon

Bron, , France

Site Status

Countries

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France

Facility Contacts

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Philippe MOULIN, Pr

Role: primary

04 72 68 13 04

Philippe DOUEK, Pr

Role: backup

Other Identifiers

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69HCL19_0931

Identifier Type: -

Identifier Source: org_study_id

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