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Clinical Trials/NCT04085614
NCT04085614CompletedNot Applicable

Dynamic Coronary Roadmap for Contrast Reduction

Philips Clinical & Medical Affairs Global6 sites in 4 countries371 target enrollmentStarted: October 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
371
Locations
6
Primary Endpoint
Total Percutaneous Coronary Intervention (PCI) Iodinated Contrast Volume

Study Overview

Brief Summary

The Dynamic Coronary Roadmap is a commercially available product developed by Philips Medical Systems, a Philips Healthcare company. Dynamic Coronary Roadmap is a software medical device intended to provide a real-time and dynamic angiographic roadmap of coronary arteries. The angiographic roadmap is automatically generated from previously acquired coronary angiograms during the same procedure. Dynamic Coronary Roadmap overlays the angiographic roadmap on live 2D fluoroscopic images, thereby assisting the physician in navigating devices, e.g. (guide) wires, catheters, through the coronary arteries.

This is a multi-center, prospective, unblinded, stratified 1:1 randomized controlled trial to assess whether using Dynamic Coronary Roadmap reduces the total iodinated contrast volume related to Percutaneous Coronary Intervention (PCI) compared to the control group without Dynamic Coronary Roadmap.

Detailed Description

Primary objective:

• To assess whether using Dynamic Coronary Roadmap reduces the total iodinated contrast volume related to Percutaneous Coronary Intervention (PCI) compared to the control group without Dynamic Coronary Roadmap.

Secondary objective:

• To assess the total number of contrast enhanced cine angiographic X-ray runs (angiograms) related to Percutaneous Coronary Intervention (PCI) in the Dynamic Coronary Roadmap and control group

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Subject is undergoing Percutaneous Coronary Intervention (PCI) with a degree of complexity that anticipates the need for more than 25ml of iodinated contrast volume
  • •Subject has signed informed consent
  • •Subject is 18 years of age or older, or of legal age to give informed consent per state or national law

Exclusion Criteria

  • •Subject undergoing emergency Percutaneous Coronary Intervention (PCI)
  • •Subject with ST-segment Elevation Myocardial Infarction (STEMI)
  • •Subject with Chronic Total Occlusion (CTO)
  • •Subject undergoing PCI for isolated ostial disease of Left Main Coronary Artery (LMCA) or Right Coronary Artery (RCA)
  • •Subject undergoing Percutaneous Coronary Intervention (PCI) with Optical Coherence Tomography (OCT) support
  • •Subject undergoing Percutaneous Coronary Intervention (PCI) with rotational or orbital atherectomy
  • •Subject with Chronic Kidney Disease (CKD) stage V (estimated Glomerular Filtration Rate (eGFR) < 15 ml/min/1.73 m^2)
  • •Subject with contrast allergy that cannot be adequately pre-medicated
  • •Subject participates in a potentially confounding drug or device trial during the course of the study.
  • •Subject is under 18 years of age, or pregnant woman, or breast feeding woman, or meets an exclusion criteria according to national law

Arms & Interventions

Dynamic Coronary Roadmap group

Experimental

Patients will be treated via standard of care for Percutaneous Coronary Intervention (PCI) with navigation support of Dynamic Coronary Roadmap.

Intervention: Percutaneous Coronary Intervention (PCI) with Dynamic Coronary Roadmap (Device)

Control group

Active Comparator

Patients will be treated via standard of care for Percutaneous Coronary Intervention (PCI) without navigation support of Dynamic Coronary Roadmap.

Intervention: Percutaneous Coronary Intervention (PCI) without Dynamic Coronary Roadmap (Device)

Outcomes

Primary Outcomes

Total Percutaneous Coronary Intervention (PCI) Iodinated Contrast Volume

Time Frame: During Percutaneous Coronary Intervention (PCI) procedure

Average total undiluted contrast volume (in ml, measured by an automatic contrast injector) per Percutaneous Coronary Intervention (PCI), where the start of the PCI is marked by the moment the interventional guiding catheter is positioned in a stable coronary position and the end of the PCI is marked by time of the last PCI check exposure run (angiogram).

Secondary Outcomes

  • Number of Angiograms(During Percutaneous Coronary Intervention (PCI) procedure)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (6)

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