Safety and Efficacy Study of the DANUBIO Paclitaxel Eluting Balloon in In-Stent Restenosis Lesions (DEBREST)
NCT01485068
Arterial Occlusive Diseases, Arteriosclerosis
Antony, France
View Trial DetailsNCT Number: NCT07391033
To compare the angiographic and clinical outcomes of aggressive versus standard balloon preparation during drug-coated balloon (DCB) angioplasty for in-stent restenosis (ISR). The study will evaluate whether more aggressive lesion preparation with cutting/scoring/OPN balloons improves outcomes compared to standard preparation with semi-compliant or non-compliant balloons.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
PICCOLETO XI A-PREP is an investigator-initiated, multicenter, international, observational study evaluating the impact of lesion preparation strategies on outcomes following drug-coated balloon (DCB) angioplasty for in-stent restenosis (ISR).
In-stent restenosis remains a clinically relevant challenge despite advances in drug-eluting stent technology and contemporary percutaneous coronary intervention techniques. DCB represents a stentless therapeutic strategy for ISR treatment, with the advantage of avoiding implantation of additional metallic layers.
A key determinant of clinical outcomes in ISR, particularly with DCB angioplasty, is the adequacy of lesion preparation before definitive therapy. Effective preparation facilitates optimal drug delivery, improves luminal gain, and may reduce the risk of recurrent restenosis.
A large spectrum of balloon-based modalities is available for ISR lesion preparation, ranging from semi-compliant and non-compliant balloons to more aggressive tools such as scoring and cutting balloons. Although more aggressive devices may enhance plaque modification and neointimal tissue disruption, their incremental clinical benefit over standard approaches remains uncertain.
Patients will be categorized into two groups based on lesion preparation strategy:
Clinical outcomes will be assessed at 1-year and longest available follow-up.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 12 months
Composite of cardiac death, non-fatal myocardial infarction (MI), or target lesion revascularization (TLR).
Time frame: 12 months and longest available follow-up
Death attributed to cardiovascular causes, including death from unknown cause.
Time frame: 12 months and longest available follow-up
Non-fatal myocardial infarction according to the Fourth Universal Definition of Myocardial Infarction.
Time frame: 12 months and longest available follow-up
Any repeat revascularization (percutaneous or surgical) of the target lesion.
Time frame: 12 months and longest available follow-up
Myocardial infarction attributable to the target vessel based on clinical, electrocardiographic, and biomarker criteria.
Time frame: 12 months and longest available follow-up
Bleeding Academic Research Consortium (BARC) major bleeding events (type 3-5).
Time frame: At procedure
Successful DCB angioplasty with residual stenosis less than 30% and TIMI flow grade 3 without major procedural complications.
Time frame: At procedure
Percentage of diameter stenosis after DCB angioplasty assessed by quantitative coronary angiography.
Time frame: At procedure
Presence and type of coronary dissection after lesion preparation and DCB treatment.
Time frame: At procedure
Thrombolysis In Myocardial Infarction (TIMI) flow grade assessment post-procedure.
Contact information is provided by the study sponsor or research team.
Beatrice Barbano
CONTACT
Filippo Luca Gurgoglione, MD, PhD
CONTACT
Fondazione Ricerca e Innovazione Cardiovascolare ETS
Other
Impact of Lesion PREParation With Modifying Balloons During Drug-coated Balloon (DCB) Angioplasty for In-stent Restenosis (ISR) - PICCOLETO XI A-PREP Study
Acronym: PICCOLETO-XI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT01485068
Arterial Occlusive Diseases, Arteriosclerosis
Antony, France
View Trial DetailsNCT00961181
In-Stent Coronary Artery Restenosis
Freiburg im Breisgau, Germany
View Trial DetailsNCT01296399
In-Stent Coronary Artery Restenosis
Haifa, Israel
View Trial DetailsNCT07730528
Arterial Occlusive Diseases, Arteriosclerosis
View Trial Details