- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07855614
OPTIMized Diagnosis and Treatment System Based on AI and Multimodal Imaging Fusion for PCI (OPTIMAI-PCI) (OPTIMAI-PCI)
An Optimized Diagnosis and Treatment System Based on Artificial Intelligent and Multimodality Imaging Fusion for Percutaneous Coronary Intervention: a Prospective and Multicenter Study
This study compares an AI-based imaging fusion guidance system with standard intravascular ultrasound-guided PCI in adults with complex coronary artery lesions. The system combines angiography and intravascular ultrasound to help physicians plan and optimize stent placement. The study will assess whether the system improves immediate post-procedure vessel function and stent optimization without increasing safety risks.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
This prospective, multicenter, randomized, controlled superiority study will enroll adults undergoing PCI for complex non-left-main coronary artery lesions. Participants will be randomized 1:1, stratified by study center, to standard IVUS-guided PCI or PCI assisted by an AI-based imaging fusion guidance system. Both groups will receive standard PCI and peri-procedural care. The primary composite outcome is immediate target-vessel optimization after PCI, defined by post-PCI micro quantitative flow ratio of at least 0.90, minimum stent area of at least 5.0 mm2, and no major stent-edge failure. Clinical follow-up will occur at 1, 6, and 12 months to assess target-vessel failure and safety events.
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Changqing Du
- Telefonnummer: +86-13656680012
- E-post: ddcq82@126.com
Studiesteder
-
-
Zhejiang
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Hangzhou, Zhejiang, Kina
- Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
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Hangzhou, Zhejiang, Kina
- Zhejiang Hospital
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Hangzhou, Zhejiang, Kina
- Affiliated Hospital of Hangzhou Normal University
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Hangzhou, Zhejiang, Kina
- First Affiliated Hospital, Zhejiang University School of Medicine
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Hangzhou, Zhejiang, Kina
- Hangzhou First People's Hospital affiliated with Westlake University School of Medicine
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Hangzhou, Zhejiang, Kina
- Second Affiliated Hospital, Zhejiang University School of Medicine
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Yuhuan, Zhejiang, Kina
- Yuhuan Second People's Hospital
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Zhoushan, Zhejiang, Kina
- Zhoushan Hospital
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Age 18 to 80 years, inclusive, at the time of informed consent.
- Planned PCI for a target non-left-main coronary lesion meeting at least one of the following: typical myocardial ischemic symptoms with angiographic stenosis >70%; atypical symptoms with angiographic stenosis >=90%; functional measurement by FFR or QFR <0.80; or minimum lumen area below the protocol threshold for vessel diameter (<2.4 mm2 for <3.0 mm, <2.7 mm2 for 3.0-3.5 mm, or <3.6 mm2 for >3.5 mm).
- Complex coronary lesion: a single diffuse long lesion >20 mm or tandem lesions separated by >10 mm of non-diseased vessel.
- Participant or legally authorized representative can understand and sign written informed consent, can follow study procedures, and agrees to required contraception during the study.
Exclusion Criteria:
- Allergy or contraindication to heparin, aspirin, P2Y12 receptor antagonists, or contrast media, except contrast allergy controllable by premedication.
- Active pathologic bleeding or gastrointestinal or genitourinary bleeding within 3 months before PCI.
- Bleeding tendency or known coagulation disorder, including heparin-induced thrombocytopenia.
- Life expectancy <1 year or inability to comply with the protocol, in the investigator's judgment.
- Bypass graft lesion, left-main or unprotected left-main coronary lesion.
- STEMI within 24 hours of symptom onset or cardiogenic shock at admission (Killip class IV).
- Uncontrolled severe systemic disease, including severe hepatic, renal, hematologic, or psychiatric disease; examples include ALT or AST >3 times the upper limit of normal, total bilirubin >1.5 times the upper limit of normal, albumin <35 g/L, cirrhosis or uncontrolled ascites, eGFR <30 mL/min/1.73 m2 or dialysis, platelet count <50 x 10^9/L, hemoglobin <80 g/L, hemolytic anemia, or aplastic anemia.
- Pregnant or breastfeeding participant, or plans for pregnancy or breastfeeding during the study.
- Target-vessel PCI within 12 months or in-stent restenosis.
- Severe calcified lesion or major epicardial coronary ostial lesion expected to require atherectomy pretreatment.
- IVUS catheter cannot cross the lesion.
- Angiographic image quality inadequate for muQFR analysis, including severe overlap, insufficient projections, or poor contrast filling.
Withdrawal and Exclusion from Per-Protocol Analysis:
- PCI not performed after randomization or key imaging missing and not recoverable; participant remains in the intention-to-treat set where applicable.
- Withdrawal of informed consent.
- Investigator judges continued participation may endanger the participant, such as a serious adverse event or very poor compliance.
Recruitment:
Participants will be screened among inpatients and outpatients scheduled for PCI for complex coronary lesions at participating centers. Investigators will explain the study and obtain written informed consent before enrollment.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Aktiv komparator: Standard IVUS-Guided PCI
Standard percutaneous coronary intervention guided by intravascular ultrasound according to current clinical guidelines, including pre-procedural assessment, stent selection, and post-procedural optimization. |
Percutaneous coronary intervention guided by intravascular ultrasound according to current clinical guidelines, including pre-procedural imaging assessment, stent selection, and post-procedural optimization. |
|
Eksperimentell: Imaging Fusion-Guided PCI
Standard percutaneous coronary intervention with use of the AI-based imaging fusion guidance system for ICA-IVUS fusion, virtual stent planning, stent recognition and reconstruction, quantitative assessment of expansion and apposition, and edge-complication alerts. |
Percutaneous coronary intervention guided by intravascular ultrasound according to current clinical guidelines, including pre-procedural imaging assessment, stent selection, and post-procedural optimization. AI-based software device for real-time fusion of coronary angiography and intravascular ultrasound during PCI. It supports virtual stent planning, stent recognition and reconstruction, quantitative evaluation of stent expansion and apposition, detection of edge complications, and functional assessment support including micro quantitative flow ratio. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Immediate Post-PCI Target-Vessel Composite Optimization Success
Tidsramme: Immediately after PCI (0 hours, before leaving the catheterization laboratory)
|
Proportion of participants whose target vessel simultaneously meets all three core-laboratory-assessed criteria after final PCI optimization: post-PCI micro quantitative flow ratio (muQFR) >=0.90; minimum stent area (MSA) >=5.0 mm2; and no major stent-edge failure. Major edge failure is defined as longitudinal geographic mismatch (plaque burden >=50% within 5 mm proximal or distal to the stent edge) and/or a major edge dissection involving the media and >3 mm in length. |
Immediately after PCI (0 hours, before leaving the catheterization laboratory)
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Target Vessel Failure (TVF) through 12 Months
Tidsramme: 1 month, 6 months, and 12 months after PCI; event-triggered assessment throughout follow-up
|
Composite of cardiac death, target-vessel myocardial infarction, or ischemia-driven target-vessel revascularization. Suspected events will be adjudicated by the blinded Clinical Events Committee. Stent thrombosis will also be recorded. |
1 month, 6 months, and 12 months after PCI; event-triggered assessment throughout follow-up
|
|
Peri-Procedural and In-Hospital Safety Events
Tidsramme: From PCI through hospital discharge or 30 days, whichever occurs first
|
Incidence of bleeding events, contrast-associated adverse reactions, vascular access-site complications, peri-procedural myocardial infarction or acute vessel closure, serious adverse events, and other clinically significant adverse events during PCI and hospitalization. |
From PCI through hospital discharge or 30 days, whichever occurs first
|
|
12-Month Safety Outcomes
Tidsramme: 1 month, 6 months, and 12 months after PCI; event-triggered assessment throughout follow-up
|
Incidence of serious adverse events, bleeding, stent thrombosis, stroke or systemic embolism, repeat hospitalization, and medication-related adverse reactions during follow-up. |
1 month, 6 months, and 12 months after PCI; event-triggered assessment throughout follow-up
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Changqing Du, Zhejiang Hospital
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- ZJHIRB-2026-034K
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Individual participant data will not be shared because the data include sensitive personal health information, and the currently approved informed consent and ethics documents do not authorize external sharing of participant-level data.
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