Atherectomy Clinical Trials

Clinical trials related to Atherectomy Procedure

A Randomized Controlled Multicentric Trial to Assess Non-inferiority of an Orbital Atherectomy Only Versus a Calcium-tailored Debulking Approach

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Some patients with coronary artery disease have severely calcified vessels. In these cases, placing a stent - a small tube that helps keep the artery open - can be very difficult. Calcium build-up in the artery wall may prevent the stent from expanding properly, increasing the risk of complications or failure of the treatment. To prepare these vessels before stenting, doctors use special techniques to modify or remove the calcium. These techniques are known as plaque modification strategies and can include devices such as atherectomy systems, scoring balloons, or intravascular lithotripsy. However, there is no clear standard as to which strategy is best. Purpose of the Study: This study compares two different approaches to treating calcified coronary arteries before stenting: * A uniform approach using only the orbital atherectomy system (Diamondback 360®, Abbott), which sands away the calcium with a rotating crown * A tailored approach, where the operator chooses from various available methods (e.g., rotational atherectomy, scoring or cutting balloons, or shockwave therapy) based on the patient's specific type of calcium The goal is to determine whether the uniform orbital atherectomy approach is not worse (non-inferior) than the individualized method when it comes to how well the stent expands inside the artery. This is a randomized, controlled clinical trial. Patients will be randomly assigned to one of the two groups. Randomization ensures fair comparison between both groups. The decision to implant a stent and to use additional techniques is at the discretion of the interventional cardiologist.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 Years

• Chronic coronary syndrome with a clinical indication for percutaneous coronary intervention of a severely calcified lesion as defined by coronary computer tomography (CT; Agatston Score of target lesion ≥453 OR Calcium Arc \>270°). The determination of calcification in the target lesion is based on native and contrast enhanced CT scans that are conducted as per clinical guidelines. The CT images must not be older than 6 months at the time of patient enrollment.

• Signed informed consent

• The patient is an appropriate candidate for bypass surgery, angioplasty, or atherectomy therapy

Locations
Other Locations
Germany
Universitäres Herz - und Gefäßzentrum, Unversitätsklinikum Frankfurt
RECRUITING
Frankfurt
Contact Information
Primary
Marcel Kunadt, Dr.
orfita@ihf.de
+49 621 59577 223
Backup
Jelena Weller
Time Frame
Start Date: 2025-10-30
Estimated Completion Date: 2027-03
Participants
Target number of participants: 310
Treatments
Experimental: Debulging with the orbital atherectomy system (Diamondback 360®)
Active_comparator: Debulging with various available methods
Sponsors
Leads: IHF GmbH - Institut für Herzinfarktforschung

This content was sourced from clinicaltrials.gov