Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT01943643 |
Other study ID # |
ZEM - CARD - 001 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
September 2013 |
Est. completion date |
July 2018 |
Study information
Verified date |
June 2023 |
Source |
Clinical Hospital Center Zemun |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
This is prospective, observational study, that will be conducted in two high-volume
university interventional cardiology centers. Study population consists of patients with
"true" coronary bifurcations (Medina 1.0.1; 0.1.1; 1.1.1) with >50% stenosis in both main
(MB) and side branch (SB). Patients are scheduled to undergo percutaneous coronary
intervention (PCI) based on clinical findings. Before PCI, patients will undergo multislice
CT angiography (MSCTA). MSCTA before PCI for "true" non left main bifurcation lesions can
determine atherosclerotic plaque characteristics in MB and SB and predict significant
narrowing of SB after provisional stenting. Primary goal is to determine which plaque
characteristics of "true" non left main bifurcation lesions in MB and SB, as assessed by
MSCTA, can affect the occurrence of SB ostial compromise after provisional stenting. Patients
will be seen in the office visit at 1, 3, 6 and 12 months after the procedure. Clinical
evaluation and 12-channel ECG are mandatory at each visit. Comprehensive echocardiogram with
2D-strain analysis will be done at 3-month visit. Repeated coronary angiography will be done
at 6-month visit, and will include quantitative analysis of previously treated bifurcation
lesion.
Description:
This is prospective, observational study, that will be conducted in two high-volume
university PCI centers. The centers are: Clinical Hospital Center Zemun-Belgrade, Cardiology
Department, and Clinical Center of Serbia, Cardiology Clinic. Study population consists of
patients with "true" coronary bifurcations (Medina 1.0.1; 0.1.1; 1.1.1) with >50% stenosis in
both MB and SB9. Patients are scheduled to undergo PCI based on clinical findings. Before
PCI, patients will undergo MSCTA. Study hypothesis is that MSCTA before PCI for "true" non
left main bifurcation lesions can determine atherosclerotic plaque characteristics in MB and
SB and predict significant narrowing of SB after provisional stenting. Primary goal is to
determine which plaque characteristics of "true" non left main bifurcation lesions in MB and
SB, as assessed by MSCTA, can affect the occurrence of SB ostial compromise after provisional
stenting. Plaque characteristics that will be investigated include: angle between the
arteries, the degree of stenosis, length of stenosis, density of the plaque, plaque volume,
positive remodeling of the artery, and presence of spotty calcifications.
Secondary aims are to determine whether MSCTA correctly identifies the degree of stenosis and
atherosclerotic plaque composition in MB and SB of bifurcation lesions compared to invasive
quantitative coronary angiography and IVUS. Also to determine correlation between endothelial
wall shear stress, computed using mathematical model of fluid dynamic reconstruction of MSCTA
findings, and the degree of stenosis and atherosclerotic plaque composition in MB and SB of
bifurcation lesion. Another goal is to determine correlation between SB stenosis and coronary
blood flow after provisional stenting and regional myocardial function assessed by myocardial
deformation imaging echocardiography in the area of the left ventricle supplied by SB,
immediately after intervention, and after three months. Study patients will be selected based
on previous diagnostic coronary angiogram. They will undergo MSCTA on Toshiba Aquilion CXL
128 slice CT scanner using predefined protocol. The procedure will include calcium scoring
(Agatston) then CT angiography using Ultravist 370 contrast agent ((iopromide concentration
370 mg/ml, Bayer Health Care, Germany). MSCTA angiograms will be analyzed using dedicated
software Vital Vitrea Advanced 6.2, Vital Images, Minnetonka, Minnesota, US. The bifurcation
lesion analyses will include: the measurement of the angle between MB and SB, measurement of
the lesion length, reference diameter of the vessel, degree of stenosis, atherosclerotic
plaque analysis 10 mm proximal and distal in the MB, and 5 mm from the ostium of the SB, and
at the level of maximum stenosis (minimal lumen diameter).
Plaque analyses will include:
1. Type of tissue based on density: lipid, fibro-lipid or calcified,
2. Plaque volume at the level of bifurcation
3. Positive remodeling of the artery at the level of bifurcation
4. Presence of spotty calcification. Before PCI procedure, IVUS evaluation using iLab®
Ultrasound Imaging System (Boston Scientific, Natick, Massachusetts, US), of the MB and,
if possible, the SB will be performed. Automated pullback at 0.5 mm/s will be used to
evaluate both branches before the PCI procedure.
Initial strategy for PCI will be provisional stenting. The choice of vascular access, guiding
catheters and coronary wires are left to the operators' discretion. Heparin in doses of
80-100 IU/kg will be used as periprocedural anticoagulation. After placing the guidewires in
the MB and SB lesion, the MB will be predilated. After predilation and nitroglycerin
administration intracoronary, coronary angiogram will be performed. Based on this angiogram,
a second generation drug eluting stent (DES) will be placed in the MB across the SB, so that
its diameter will be chosen according to Murray's law. The stent will have to be long enough
so that proximal margin of the stent is at least 10 mm proximal to the carina of the
bifurcation. After stenting, proximal optimization (POT) of the stent in the MB will be
performed using short noncompliant balloon catheter 0,5 mm larger than the diameter of the
stent. The distal marker of the balloon catheter will be positioned at the level of carina.
Inflation of the balloon catheter must be at least up to the nominal diameter. After POT and
intracoronary nitroglycerin administration, coronary angiograms in two orthogonal projections
will be done. If the SB does not have more than 75% diameter stenosis (DS) on quantitative
coronary angiography analysis (QCA) and/or coronary blood flow less than TIMI III, the
procedure is finished. If the SB has more than 75% DS stenosis or TIMI flow