Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06736899

Trial of Orbital Atherectomy Versus Standard Strategy in Calcified Bifurcation Lesions

Clinical research with medical devices indicated in accordance with the CE marking, led by researchers, multicenter, open, prospective, randomized and controlled. Patients are randomized to treatment with a conventional balloon and then a coronary stent or to initial plaque modification with Orbital Atherectomy (OA) and then a coronary stent. To evaluate the efficacy and safety of OA in the adequate treatment with coronary stent of the calcified bifurcation lesion using angiography and optical coherence tomography (OCT).

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

H. G.U. de ALICANTE DR. BALMIS, Alicante, Spain

Loading trial locations.

About this study

The risk profile of patients and their comorbidities have worsened and the observed lesions undergoing treatment are increasingly complex. This has promoted the development of new technologies for plaque modification, especially in the context of calcified lesions. These predispose to suboptimal results of the intervention due to an increased risk of malapposition and underexpansion of the stents, the main variables for restenosis and/or thrombosis of the stents. Thus, compared with non-calcified lesions, the increased amount of calcium in the coronary artery leads to a higher incidence of major adverse cardiac events (MACE).

Coronary bifurcation stenting remains complex and is associated with a high risk of stent thrombosis and restenosis even with contemporary techniques, and suboptimal outcomes are frequently observed due to side branch (SL) involvement that increases cardiovascular events.

Our hypothesis is that the use of orbital atherectomy (OA) for coronary revascularization in the presence of calcified bifurcation lesions is feasible and safe compared to the more common technique, favoring the subsequent performance of provisional stenting (PS).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients over 18 years of age and
  • Patients with moderately or severely calcified bifurcation lesions (lateral vessel ≥ 2mm), candidates for PCI with coronary stent implantation, in whom there is the possibility of adequate clinical follow-up at 1 year and
  • Patients agree to participate in the study, by signing the Informed Consent.

Exclusion criteria

  • Patients with revascularization of the artery to be treated within 9 months prior to the index procedure.
  • Patients with contraindication for the use of Orbital Atherectomy:
  • Patients in cardiogenic shock.
  • Patients with Thrombotic lesions.
  • Patients with Vascular graft disease.
  • Patients with remain vessel disease.
  • Patients with severe left ventricular dysfunction.
  • Patients allergic to the components of the washing serum (glide).
  • Patients with life expectancy less than one year.

Treatment and study plan

Orbital Atherectomy System Treatment

Device

Percutaneous coronary intervention of a calcified bifurcation coronary lesion with balloon angioplasty followed by drug eluting stent. Selection of balloon type is at operator´s discretion. Baseline and post dilation OCT will be performed.

Balloon System Treatment

Device

Percutaneous coronary intervention of a calcified bifurcation coronary lesion with Orbital Atherectomy followed by drug eluting stent. Baseline and post dilation OCT will be performed.

Primary outcomes

  1. EFFICACY: Angiographic criteria success

    Time frame: At the end of PCI (Percutaneous Coronary Intervention)

    Percentage of Main vessel and side branch (≥2 mm) patency (final stenosis <20%) without the presence of: residual lesion >70% and TIMI flow < 3 and residual ≥ type C disection

  2. EFFICACY: OCT criteria: Stent expansion

    Time frame: At the end of PCI

    Percentage of MLA / mean reference luminal area (mean proximal and distal reference luminal)

Secondary outcomes

  1. SAFETY:Major adverse cardiac events (MACE)

    Time frame: 12 months

    Rate of cardiac death, myocardial infarction (MI), target lesion revascularization (TLR), and non-target lesion target vessel revascularization (TVR non-TLR), thrombosis and stroke

  2. SAFETY:Major adverse cardiac events (MACE)

    Time frame: 6 months

    Rate of cardiac death, myocardial infarction (MI), target lesion revascularization (TLR), and non-target lesion target vessel revascularization (TVR non-TLR), thrombosis and stroke

  3. SAFETY:Major adverse cardiac events (MACE)

    Time frame: 30 days

    Rate of cardiac death, myocardial infarction (MI), target lesion revascularization (TLR), and non-target lesion target vessel revascularization (TVR non-TLR), thrombosis and stroke

  4. SAFETY:Major adverse cardiac events (MACE)

    Time frame: At the end of PCI

    Rate of cardiac death, myocardial infarction (MI), target lesion revascularization (TLR), and non-target lesion target vessel revascularization (TVR non-TLR), thrombosis and stroke

  5. EFFICACY: Other variables related to stent expansion. Minimal Lumen Area (MLA) in mm2

    Time frame: At the end of PCI

    Cut-off point >5 mm2

  6. EFFICACY: Other variables related to stent expansion. Minimal Lumen Area (MLA)

    Time frame: At the end of PCI

    Percentage of Cut-off point >90 mm2

  7. EFFICACY: Other variables related to stent expansion. Mean stent expansion

    Time frame: At the end of PCI

    Percentage of mean stent area (sum of stent area/analyzed stent length)/mean reference lumen area (cut-off point>80%)

  8. EFFICACY: Other variables related to stent expansion. Stent expansion using linear model

    Time frame: At the end of PCI

    Percentage of stent volume/adaptative reference lumen volume. (cut-off point>65%)

Study contacts

Contact information is provided by the study sponsor or research team.

FUNDACION EPIC

CONTACT

[email protected]

0034987876135

JORGE PALAZUELOS, MD, PhD

CONTACT

[email protected]

0034659768506

Sponsors and collaborators

Lead sponsor

Fundación EPIC

Other

Registry information

Official study title

Randomized Trial of Orbital Atherectomy Versus Standard Strategy in Calcified Bifurcation Lesions

Acronym: OraBil

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 17, 2024
Registry last updated
Jul 8, 2026

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.