The OSTIAL Study (Optimization of Stent Placement in Aorto-ostial Lesions)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Cardiologique du Nord

About this trial

Aorto-ostial coronary lesions present a significant challenge during coronary angioplasty. This is due to the difficulty of precisely identifying the aorto-ostial plane and the frequent instability of the guiding catheter during stent deployment.

Despite the angiographic appearance being deemed optimal, several studies have shown a high rate of suboptimal stent positioning at the ostium when subsequent coronary CT angiography (CCTA) assessment is performed.

This suboptimal positioning may be linked to incomplete ostial coverage, which could increase the risk of in-stent restenosis. It may also be linked to excessive stent protrusion into the aorta, which could compromise future procedures, particularly in the context of transcatheter aortic valve replacement.

The "Floating Balloon" (FB) technique has been developed to improve system stability and to reliably mark the aorto-ostial landing zone (AOLZ). A previous study demonstrated the feasibility and accuracy of this technique.

The aim of the current study is to assess the clinical effectiveness of the Floating Balloon. Although this technique is already in use, no study has yet conducted a systematic assessment of stent positioning using CCTA.

The study utilised a combined retrospective-prospective approach to comprehensively evaluate the incidence of suboptimal stent positioning associated with the Floating Balloon technique. This evaluation was conducted by systematically comparing patient outcomes between those treated with the FB and those treated without the FB. The study employed CCTA as a key tool to assess stent position, ensuring a precise analysis of the data.

To achieve this, it is recommended that follow-up data from patients who have already undergone the FB procedure and had their stent position assessed via CCTA (retrospective component) be analysed, while also enrolling new patients and randomizing them into FB and non-FB groups (prospective component).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female aged over 18 years

Prospective part: Patient who has signed an informed consent form

Retrospective part: No objection to the use of personal data for this research

Indication for coronary angioplasty for an aorto-ostial lesion (right coronary artery or left main coronary artery) for patients included in the prospective part / Patients in the historical part who underwent coronary angioplasty for an aorto-ostial lesion (right coronary artery or left main coronary artery) using the "floating balloon" (FB) technique, followed by a CCTA assessment of positioning

Disqualifiers

Contraindication to coronary CT angiography (severe renal impairment not requiring dialysis (GFR ≤ 30 ml/min)), applicable only to patients included in the prospective part

Refusal of consent (patients included in the prospective part)

Objection to the use of personal data (patients in the retrospective part)

Patient unable to read, write, or understand French

Trial design

Design model

Parallel

Treatments tested in this trial

  • Coronary angioplasty using the floating balloon technique

    Procedure/Surgery

    Coronary angioplasty using the FB technique involves the following steps: 1. Crossing the aorto-ostial lesion using a standard coronary guidewire positioned in the target artery. 2. Withdrawing the guiding catheter from the ostium and placing a second guidewire, formed into a loop, within the aortic root. 3. Inflating a small-diameter (2 mm) balloon in the aorta over the second guidewire; this serves as the "floating balloon." 4. Advancing the stent toward the target lesion. 5. Gradually withdrawing the floating balloon until its proximal marker contacts the tip of the guiding catheter, thereby defining the aorto-ostial plane and the aorto-ostial landing zone (AOLZ). 6. Maintaining forward pressure on the guiding catheter to stabilize the entire system and limit selective engagement of the ostium. 7. Aligning the stent's proximal marker with the balloon marker and the tip of the guiding catheter, followed by gradual deployment of the stent.

  • Coronary angioplasty without the floating-balloon technique

    Procedure/Surgery

    Angioplasty of the aorto-ostial lesion without the jailed-balloon (FB) technique will be performed as follows: 1. Coronary catheterization via the access route chosen by the operator 2. Predilatation, if deemed necessary 3. Implantation of a drug-eluting stent (DES) sized according to angiographic or QCA assessment 4. Final optimization (post-dilatation, POT, or other techniques) at the operator's discretion

Treatment groups

75 Participants
are divided into 2 treatment groups
Group A: Coronary angioplasty using the floating balloon techniqueExperimental treatment 1 intervention
Group B: Coronary angioplasty without the floating-balloon techniqueActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

The number of participants in whom stent placement was technically successful and who were evaluated by CT scan.

Time frame
At the end of the procedure

Secondary outcomes

1

The secondary outcome is the rate of major adverse cardiovascular events (MACE).

The secondary outcome is the rate of major adverse cardiovascular events (MACE), including cardiac mortality, all-cause mortality, myocardial infarction (MI), target lesion revascularization (TLR) and hospitalisation for cardiovascular causes.

Time frame
12 months after the surgery procedure

Other outcomes

Sponsors and contacts

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