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Coronary Revascularisation by rePOT

Coronary Artery Bifurcation Revascularization Without kIssing ballOon infLation by rEpoT: The CABRIOLET Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03550196
Acronym
CABRIOLET
Enrollment
500
Registered
2018-06-08
Start date
2018-05-14
Completion date
2022-06-23
Last updated
2024-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Brief summary

The presence of a coronary bifurcation complicates percutaneous revascularization. Bifurcation stenting needs to take into account the difference of diameter between proximal and distal vessels and the necessity to limit the side branch obstruction. Provisional stenting techniques with balloon juxtaposition as Kissing Balloon Inflation (KBI) fail to demonstrate a clinical benefits. This is probably explain by the detrimental effect during these technics on the proximal segment with an arterial overstretch. A new sequential technique, named rePOT, demonstrated experimentally a mechanical superiority compared to juxtaposition balloon techniques included KBI. RePOT associates an initial proximal optimizing technique (POT), a side branch inflation and a final POT. A first clinical study (n=106 patients) confirmed these excellent mechanical results with serial OCT analysis and demonstrated an excellent short term safety. Since 2017, rePOT is recommended in Europe in clinical practice. This large registry is dedicated to confirm the clinical benefits at long term after bifurcation revascularization with rePOT technique before a large randomise trial.

Interventions

OTHERProvisional stenting with rePOT technique

All revascularizations have to be performed with complete rePOT technique: initial POT + side branch inflation + final POT. Compliant or semi compliant balloon have to be preferred to inflations. The POT balloon positioning have to be precise as obtain the loose of the parallelism just at the carina cut plan. The rest of the medication or procedure characteristics stay at the discretion of the operator. The follow-up will be clinic every years.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Discovery, during angiography, of a significant coronary lesion (by angiographic or functional assessment) including a bifurcation under a provisional stenting strategy. Bifurcation have to be significant according to the operator and the coronary anatomy (but the side branch diameter have to be greater than 1.75mm) * Stable lesion without high thrombus burden * Patient agreement to study participation and ≥ 18 years

Exclusion criteria

* Complex lesion or anatomy requiring revascularization strategy with more than one stent * Contraindication to a double platelet anti-aggregation ≥ 6mois (recommended implantation of active stent) * Unstable patient according to the operator (used of hemodynamic drug support, mechanical ventilation) * Indication of cardiac surgery. * Lesion culprit in ST- or non ST-elevation myocardial infarction \<12h. * High thrombus burden in angiography or endocoronary imaging (IVUS, OCT). * Pregnancy, loose of legal right * Other interventional study participation \<30 jours.

Design outcomes

Primary

MeasureTime frameDescription
Long-term clinical benefits after revascularization of coronary bifurcations by the technique of provisional stenting rePOT.At 12 monthsNumber of deaths

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026