Stent Placement Clinical Trials

Clinical trials related to Stent Placement Procedure

Clinical Impact of Intravascular Ultrasound-guided vs. Angiography-guided Coronary Stenting in Patients With Acute Coronary Syndrome: Multicenter, Randomized Control Trial (SAINT-IVUS)

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Coronary artery disease is associated with substantial morbidity and mortality worldwide. Percutaneous coronary intervention (PCI) is a pivotal procedure for the treatment of coronary artery disease. Although coronary angiography (CA) is the standard imaging modality used for coronary stent implantation, it provides only two-dimensional images of the coronary arteries. Intravascular ultrasound (IVUS) can provide additional information on plaque characteristics and vessel morphology, which may facilitate optimal stent sizing and procedural optimization. However, IVUS requires additional time and cost and may increase procedural complexity. Evidence regarding the clinical benefit of IVUS-guided PCI in patients with acute coronary syndrome (ACS) remains limited. This study is a prospective, multicenter, randomized controlled trial designed to compare IVUS-guided PCI versus angiography-guided PCI in patients with ACS. A total of 1,500 participants will be randomized 1:1 to either the IVUS-guided group or the angiography-guided group. Participants will be recruited from 15 PCI centers in Korea. The primary outcome is target vessel failure at 2 years.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Maximum Age: 90
Healthy Volunteers: f
View:

• Patients 19 years of age or older

• Patients with unstable angina pectoris, and acute MI including NSTEMI or STEMI.

• Coronary artery disease defined as \>70% stenosis (reference vessel diameter 2.5 - 5.0 mm based on operator assessment) with identifiable culprit lesion indicated stent implantation

• All lesions must be suitable for treatment with the Synergy stent system, or other Synergy platform iteration

• The patient or guardian agrees to the study protocol and the schedule of clinical and angiographic follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethical Committee of the respective clinical site.

Locations
Other Locations
Republic of Korea
The Catholic University of Korea, Eunpyeong St. Mary's Hospital
RECRUITING
Seoul
Contact Information
Primary
SUK MIN SEO, Assisted Professor
ssm530@catholic.ac.kr
82+010-9090-8491
Backup
YUN JU KANG, RN,CRC
yunju423@naver.com
82+010-7358-5252
Time Frame
Start Date: 2025-03-13
Estimated Completion Date: 2031-12-31
Participants
Target number of participants: 1500
Treatments
Experimental: IVUS-guided PCI
PCI will be performed under IVUS guidance. Post-stent IVUS assessment is mandatory, and procedural optimization will be performed according to predefined IVUS criteria. Additional balloon dilation or stent implantation may be performed at the operator's discretion if optimization criteria are not met.
Active_comparator: Angiography-guided PCI
PCI will be performed under coronary angiography guidance. Routine IVUS use is not planned. IVUS may be used only for bailout situations at the operator's discretion.
Sponsors
Leads: SUK MIN SEO
Collaborators: Boston Scientific Korea Co. Ltd

This content was sourced from clinicaltrials.gov

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