Outcomes of Different Techniques of Aortoostial Coronary Intervention Assessed by Coronary Computed Tomography Angiography

NCT ID: NCT06975930

Last Updated: 2025-05-16

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-01-01
• Study Completion Date: 2026-12-31

Brief Summary

Aorto-ostial coronary lesions (AOL) are defined as a stenosis >50% within 3 mm of the orifice of the right coronary artery (RCA) or left main coronary artery (LMCA).

The prevalence of AOL varies according to the studied population and is more common in the RCA.

Aorto-ostial lesions commonly have a unique three-dimensional funnel-shaped morphology with a variable angle of takeoff of the coronary artery from the aorta.

Percutaneous treatment of AOL is challenging due to a variety of factors which include unfavorable lesion histology, complex 3D anatomy, inability of conventional angiography to reliably delineate the aorto-ostial plane and guide the intervention and unsuitability of current tubular stent designs for this lesion subset.

Coronary computed tomography angiography (CCTA) clearly defines AOL anatomy, its relation to the aortic wall and the degree of plaque calcification.

CCTA is uniquely suited to assess the accuracy of AOL stent implantation. While conventional single wire technique is the most commonly used approach for AOL stenting, An approach uses an accessory free floating guide-wire placed within the aortic sinus to mark the aorto-ostial plane and prevent entry of the catheter into the coronary artery is called floating wire technique & is being used now.

Aim of work: 1-Comparison between 2D angiography versus Floating wire technique regarding aorto-ostial stent implantation site within the AOLZ assessed by CCTA .

2- Short term outcomes regading MACE in both groups including : myocardial infarction (MI), stroke, all-cause mortality and target vessel revascularisation (TVR).

• Type of the study: This is a randomized prospective cross sectional study
• Duration of the study: Patients will be recruited over a period of 12 months.
• Study Population: The study will include all patients who will undergo aorto-ostial coronary stenting & patients will be categorized into 2 groups Group A:patients who will undergo 2D convnetional angiography Aorto-ostial stenting.

Group B: Patients who will undergo Aorto-ostial stenting with Floating wire technique.

Patients will undergo CCTA to detect geographic miss within 6 months of stent impalntation.

Both groups will be followed up clinically to detect adverse clinical outcomes such as AMI, recurrent chest pain,….etc.

Methdos:

Optimal AOL stenting requires placement of the entire circumference of the proximal stent edge within the aorto-ostial landing zone (AOLZ), defined as the area along the axis of the coronary artery located within 1 mm of the aorto-ostial plane.

Stent geographic miss may be diagnosed when at least a segment of the circumference of the proximal stent edge is located proximal or distal to the AOLZ.

Accurate AOL stent implantation is crucial. If geographic miss was attributed to the angulated vessel take-off from the aorta preventing precise localisation of the cylindrical stent structure within the constraints of the AOLZ, it is defined as anatomy-dependent.

Geographic miss in which all aspects of the proximal stent edge extended beyond the AOLZ either proximally or distally was attributed to incorrect implantation of the stent and was defined as procedure-dependent.

Detailed Description

Aorto-ostial coronary lesions (AOL) are defined as a stenosis >50% within 3 mm of the orifice of the right coronary artery (RCA) or left main coronary artery (LMCA).

The prevalence of AOL varies according to the studied population and is more common in the RCA.

Aorto-ostial lesions commonly have a unique three-dimensional funnel-shaped morphology with a variable angle of takeoff of the coronary artery from the aorta.

Percutaneous treatment of AOL is challenging due to a variety of factors which include unfavorable lesion histology, complex 3D anatomy, inability of conventional angiography to reliably delineate the aorto-ostial plane and guide the intervention and unsuitability of current tubular stent designs for this lesion subset.

Coronary computed tomography angiography (CCTA) clearly defines AOL anatomy, its relation to the aortic wall and the degree of plaque calcification.

CCTA is uniquely suited to assess the accuracy of AOL stent implantation. Rubinshtein et al. recently analyzed cases of AOL stenting with CCTA. While review of the procedural angiograms suggested that stent positioning was satisfactory in 95% of the cases, CCTA revealed geographic miss in 87%. Sixty percent of the cases of geographic miss were classified as anatomy-dependent and 40% as procedure-dependent.

While conventional single wire technique is the most commonly used approach for AOL stenting, Szabo proposed a technique whereby an accessory guide-wire was passed through the most proximal stent cell and placed within the aorta, thereby preventing deep insertion of the stent into the vessel beyond the aorto-ostial plane.

Despite initial enthusiasm for this technique, it may lead to stent deformation and dislodgement.

A similar approach uses an accessory free floating guide-wire placed within the aortic sinus to mark the aorto-ostial plane and prevent entry of the catheter into the coronary artery.

Aim of work: 1-Comparison between 2D angiography versus Floating wire technique regarding aorto-ostial stent implantation site within the AOLZ assessed by CCTA .

2- Short term outcomes regading MACE in both groups including : myocardial infarction (MI), stroke, all-cause mortality and target vessel revascularisation (TVR).

• Type of the study: This is a randomized prospective cross sectional study
• Duration of the study: Patients will be recruited over a period of 12 months.
• Study Population: The study will include all patients who will undergo aorto-ostial coronary stenting & patients will be categorized into 2 groups Group A:patients who will undergo 2D convnetional angiography Aorto-ostial stenting.

Group B: Patients who will undergo Aorto-ostial stenting with Floating wire technique.

Patients will undergo CCTA to detect geographic miss within 6 months of stent impalntation.

Both groups will be followed up clinically to detect adverse clinical outcomes such as AMI, recurrent chest pain,….etc.

Methdos:

Study definitions … AOLZ defined as the area along the axis of the coronary artery located within 1 mm of the aorto-ostial plane.

Optimal AOL stenting requires placement of the entire circumference of the proximal stent edge within the aorto-ostial landing zone (AOLZ), defined as the area along the axis of the coronary artery located within 1 mm of the aorto-ostial plane.

Stent geographic miss may be diagnosed when at least a segment of the circumference of the proximal stent edge is located proximal or distal to the AOLZ.

Accurate AOL stent implantation is crucial. Proximal geographic miss with protrusion of the stent into the aorta may hinder future catheter access to the coronary artery. Distal geographic miss may leave part of the AOL uncovered by stent struts and increase the likelihood of restenosis.

If geographic miss was attributed to the angulated vessel take-off from the aorta preventing precise localisation of the cylindrical stent structure within the constraints of the AOLZ, it is defined as anatomy-dependent.

Geographic miss in which all aspects of the proximal stent edge extended beyond the AOLZ either proximally or distally was attributed to incorrect implantation of the stent and was defined as procedure-dependent.

All patients will be subjected to:

A. Full history taking B. Twelve lead ECG. C. Collecting baseline venous blood samples for Random blood glucose, serum urea & creatinine, Complete blood count, PT, PC & INR.

D. Echocardiography E. CA & PCI: All patients will be blindly randomized into the 2 groups with assessment of amount of dye needed & radiation dose.

After 3-6 months all patient will be subjected to new CA if possible specially if symptomatic for assessment of :- Significant ISR, need of further re-vasculariztion & difficulty of reengagment F. CCTA: To assess optimal stent implantation in AOLZ, partial or complete geographic miss.

Conditions

Coronary Interventions

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: DOUBLE

Study Groups

conventional group

patients who will undergo 2D convnetional angiography Aorto-ostial coronary stenting

Group Type: ACTIVE_COMPARATOR

Percutaneous Coronary Intervention (PCI)

Intervention Type: PROCEDURE

Patients with Aortoostial coronary lesion undergoing PCI will be blindly randomized into 2 groups Conventional group: patients who will undergo 2D convnetional angiography Aorto-ostial coronary stenting.

Floating Wire group: Patients who will undergo Aorto-ostial coronary stenting with Floating wire technique.

Floating Wire group

Patients who will undergo Aorto-ostial coronary stenting with Floating wire technique

Group Type: ACTIVE_COMPARATOR

Percutaneous Coronary Intervention (PCI)

Intervention Type: PROCEDURE

Patients with Aortoostial coronary lesion undergoing PCI will be blindly randomized into 2 groups Conventional group: patients who will undergo 2D convnetional angiography Aorto-ostial coronary stenting.

Floating Wire group: Patients who will undergo Aorto-ostial coronary stenting with Floating wire technique.

Interventions

Percutaneous Coronary Intervention (PCI)

Patients with Aortoostial coronary lesion undergoing PCI will be blindly randomized into 2 groups Conventional group: patients who will undergo 2D convnetional angiography Aorto-ostial coronary stenting.

Floating Wire group: Patients who will undergo Aorto-ostial coronary stenting with Floating wire technique.

Intervention Type: PROCEDURE

Other Intervention Names

PCI

Eligibility Criteria

Inclusion Criteria

• All patients >18 years old who have Aorto-ostial lesions and undergo Aorto-ostial stenting whether they have ACS or CCS.

Exclusion Criteria

• All patients who refused CCTA or refused participation in the study.
• Patients with previous Aorto-ostial stents.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Assiut University

OTHER

Sponsor Role: lead

Responsible Party

Abdalla Aly

Principal investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Assuit University Heart Hospital

Asyut, , Egypt

Countries

Egypt

Facility Contacts

Abdalla Aly Abdalla Aly Gamal, MSc

Role: primary

abdalla93@aun.edu.eg

00201064465194

Other Identifiers

Aorto-ostial coronary PCI

Identifier Type: -

Identifier Source: org_study_id