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Page 4 of 11  Flattery et al. Vessel Plus 2024;8:26  https://dx.doi.org/10.20517/2574-1209.2023.130


 Table 2. Randomized controlled trials of intravascular ultrasound-guided percutaneous coronary intervention compared with angiography alone in the drug-eluting stent era

 Name or   Year of   Design  Size  Primary endpoint  Clinical outcomes
 first author publication
 Unselected patients

 HOME-DES-  2010  Single center. 1:1 randomization of clinically unselected meeting   210  Incidence of MACE at 18 months,   No significant difference in event rates between study
 IVUS  insurance criteria for intravascular ultrasound (IVUS) (complex   defined as death, MI, and TLR; late stent  groups
 coronary lesions or patient characteristics)  thrombosis (ST)

 MOZART  2014  Single center. Block randomization of clinically unselected patients  83  Primary: volume of contrast used   Less total contrast used in the IVUS group. No significant
 scheduled for PCI with known risk of contrast-induced acute kidney   intraprocedurally   difference in event rates during hospitalization or at four
 injury. Guidelines provided to reduce contrast use in both arms with   Secondary: In-hospital and four-month   months
 further specific guidance for reducing contrast with IVUS   MACE (death, acute MI, unplanned
     revascularization, ST) and evidence of
     renal impairment
 Wang  2015  Single center. 1:1 consecutive randomization of patients with ST-  80  MACE rates (defined as cardiac death,   Decreased number of stents placed in the IVUS group. No
 elevation MI and high angiographic thrombus burden. IVUS group   recurrent MI, TVR, and intractable   difference in MACE rates at 12 months
 divided into low/high-risk based on IVUS findings with prespecified   myocardial ischemia) at 1, 3, 6, and 12
 criteria to decrease DES implantation in low risk  months
 ULTIMATE   2018  Multicenter. 1:1 randomization of clinically unselected patients with  1,448   Incidence of target vessel failure (TVF)   Decreased incidence of composite endpoint in IVUS group
 (1-year)  de novo coronary lesions. Chronic total occlusions, severe   at 12 months (composite of cardiac   (HR 0.53, P = 0.02). No significant difference in individual
 calcification, and inexperienced operators excluded  death, target-vessel MI, clinically driven  components of composite endpoint
     TVR)
 ULTIMATE   2021  Multicenter. 1:1 randomization of clinically unselected patients with  1,448  Incidence of TVF at 3 years, defined as in  Decreased incidence of composite endpoint in IVUS group
 (3-year)  de novo coronary lesions. Chronic total occlusions, severe   ULTIMATE 1-year study Safety endpoint  (HR 0.60, P = 0.01) driven by a decrease in clinically-driven
 calcification, and inexperienced operators excluded  of definite or probable ST  TVR. Lower incidence of definite/probable ST in IVUS
                                         group (HR 0.12, P = 0.02)
 Complex lesions

 AVIO  2013  Multicenter. 1:1 randomization of patients with stable coronary   284  Primary: in-lesion minimal lumen   No significant difference in event rates between study
 disease or unstable angina with complex lesions (> 28 mm, CTO,   diameter   groups
 bifurcation, < 2.5mm, four or more stents required)   Secondary: target lesion
     revascularization at 9 months; MACE
     (any MI, cardiac death, TVR) at 30 days,
     6, 9, 12, and 24 months
 RENOVATE  2023  Multicenter. 2:1 randomization of clinically unselected patients with  1,639   TVF (death from cardiac causes, target-  Decreased incidence of primary endpoint (HR 0.64, P =
 complex coronary disease (bifurcation, CTO, unprotected left main,  (800   vessel-related MI, or clinically-driven   0.008). No difference in death from any cause, any MI, and
 long lesions (> 38 mm stent), multivessel PCI, three+ stents, in-  IVUS)   TVR)   any repeat revascularization
 stent restenosis, severely calcified, ostial lesions)
 Chronic total occlusions
 AIR-CTO  2015  Multicenter. 1:1 randomization. Clinically unselected patients with at  230  Primary: in-stent late lumen loss   No significant difference in clinical events (composite or
 least one CTO randomized after initial lesion crossing to IVUS   Secondary: all-cause death, cardiac   individual components) at any time point, with the
 optimization or angiography alone  death, MI, TLR, TVR    exception of decreased incidence of definite/probable ST
     Safety: definite/probable ST        at 2 years in IVUS group (no difference in overall STs)

 CTO-IVUS  2015  Multicenter. 1:1 randomization stratified by center. Patients with   402  Occurrence of cardiac death   No significant difference in cardiac death. Decreased
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