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Angiographic Control Vs. Ischemia-driven Management of Patients Treated with PCI on Left Main with Drug-eluting Stents

Angiographic Control Vs. Ischemia-driven Management of Patients Undergoing Percutaneous Revascularization of the Unprotected Left Main Coronary Artery with Second-generation Drug Eluting Stents: the PULSE Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04144881
Acronym
PULSE
Enrollment
606
Registered
2019-10-30
Start date
2019-10-11
Completion date
2024-09-03
Last updated
2024-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Coronary Artery Disease, Left Main Coronary Artery Disease, Stable Chronic Angina

Brief summary

The present study aims to compare a planned angiographic control (PAC) follow-up strategy vs. conservative management for patients treated with drug-eluting stents on unprotected left main artery in a prospective, randomized setting. PAC will be performed by coronary computed tomography (CCT), to avoid the limitations of the invasive coronary angiography which is usually employed to perform PAC. The superiority of a PAC-based approach will be tested on a hard clinical end-point such as the incidence of major adverse cardiovascular events. The investigators will also assess the performance of CCT as a tool to perform PAC.

Detailed description

Given the undefined picture surrounding the appropriateness of planned angiographic control (PAC) following percutaneous coronary intervention (PCI) of the unprotected left main (ULM) with drug-eluting stents (DES), our aim is to evaluate, in a prospective, randomized, setting, the potential benefits of a PAC-based strategy vs. ischemia and symptoms driven conservative management. The disease of the native ULM is associated with an unfavorable prognostic outcome, which can be at least partially reversed by revascularization. Significant stenosis of the stented ULM caused by in-stent restenosis (ISR), however, presents some peculiar pathophysiological, flow-related and shear-stress features, which partly makes it a distinct disease as compared to native vessel atherosclerosis. Treatment of ISR, moreover, is a scarcely standardized and often complex procedure; some uncertainties still persist regarding the best strategy to treat ISR (stent-in-stent, drug-eluting balloons, dilation with conventional balloons). Computed coronary tomography (CCT) can precisely and not-invasively assess the presence of ISR in the stented ULM, without exposing the patients to the risks of invasive catheterization. CCT may provide an accurate reconstruction of the stented vessels, exposing the patients to a limited amount of contrast dye (approximately, 80-100 cc) and of radiation dose (approximately, 92 mGy). CCT has a very high negative predictive value for ISR, thus limiting the negative impact of the indiscriminate execution of invasive angiography on all patients treated by PCI of the ULM. Only patients with relevant ISR of ULM at CCT will undergo coronary angiography to confirm the presence of critical stenosis, and fractional flow reserve (FFR) and/or intravascular ultrasound (IVUS) will be performed in dubious cases. An increased rate of PCI has to be taken in to account with a PAC-based approach. However, with the accurate, stepwise selection of the patients and the lesions amenable to PCI of our study protocol, based on CCT, coronary angiography and, where necessary, FFR/IVUS, the increased rate of PCI is not expected to bear a negative prognostic impact. Based on these premises, our hypothesis is that early, appropriate, detection of ULM ISR and its subsequent treatment may positively impact patients' survival and reduce the incidence of adverse cardiovascular events. Specific aim 1: Evaluation of the effectiveness and safety of a PAC-based approach to follow-up patients treated by PCI of the ULM with DES-II Specific aim 2: Assessment of the incidence of ISR in patients undergoing PCI of the ULM with DES-II and evaluation of the diagnostic accuracy of CCT in the evaluation of ISR in the stented ULM Specific Aim 3: Assessment of the prognostic implications and safety of the PCI of ISR of the ULM detected by PAC as compared to conservative management with revascularization driven by symptoms and ischemia. For this purpose in this prospective, randomized controlled trial (RCT), patients will be enrolled following the index percutaneous revascularization of ULM with DES. Patients will be randomized in a 1:1 fashion to PAC-based management with CCT vs. symptoms and ischemia driven conservative management.

Interventions

DIAGNOSTIC_TESTcoronary computed tomography

patients randomized in this arm will perform computed coronary tomography 6 months after the index percutaneous revascularization on unprotected left main artery

Sponsors

Università degli Studi di Ferrara
CollaboratorOTHER
Ospedale San Luigi Gonzaga, Orbassano
CollaboratorUNKNOWN
Ospedale Santa Croce-Carle Cuneo
CollaboratorOTHER
Azienda USL Reggio Emilia - IRCCS
CollaboratorOTHER_GOV
AUSL Romagna Rimini
CollaboratorOTHER
University of Ferrara Department of Life Sciences and Biotechnology
CollaboratorUNKNOWN
A.O.U. Città della Salute e della Scienza
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

Patients with ULM disease treated by PCI with DES-II with the following inclusion criteria: * Age 18-85. * Glomerular filtration rate \> 30 ml/min Indication to percutaneous revascularization of ULM according to Syntax score (\< 33) or, in dubious cases, after Heart Team evaluation

Exclusion criteria

* Cardiogenic shock * Refusal or inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Major adverse cardiovascular events (MACE)18 months after the index revascularizationcomposite and mutual exclusive end point including death, cardiovascular death, myocardial infarction (MI) (excluding periprocedural MI), unstable angina (UA), stent thrombosis

Secondary

MeasureTime frameDescription
Target lesion revascularization (TLR)18 months after the index revascularizationtarget lesion revascularization including any TLR, any unplanned TLR and TLR driven by PAC
All cause deathwithin 18 months from the index revascularizationdeath from any cause occurring during follow up
stent thrombosiswithin 18 months from the index revascularizationAny stent thrombosis (definite, probable or possible)
CV deathwithin 18 months from the index revascularizationdeath from cardiovascular causes
Myocardial infarctionwithin 18 months from the index revascularizationMyocardial infarction defined as non ST elevation acute coronary syndrome (NST-ACS) or ST elevation myocardial infarction (STEMI)

Other

MeasureTime frameDescription
Renal function impairment18 months after the index revascularizationreduction of glomerular filtration rate of \>24% or end-stage chronic kidney disease
Overall bleedings18 months after the index revascularizationAny bleeding regardless of severity, defined according to Bleeding Academic Research Consortium (BARC) criteria
Major bleedings18 months after the index revascularizationBARC bleedings type III-IV-V
procedural complicationsIndex hospitalizationProcedural complications following each percutaneous coronary intervention (PCI): periprocedural MI defined, arterial access site complications, acute kidney injury
AKI2 days after CCT in the experimental armAcute kidney injury (AKI) following CCT will constitute safety end-point

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026