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Multimodality Optical and Ultrasound Intravascular Imaging for Stent Optimization and Atheroma Assessment

Multimodality Optical and Ultrasound Intravascular Imaging for Stent Optimization and Atheroma Assessment

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05753085
Acronym
MOUSA
Enrollment
0
Registered
2023-03-03
Start date
2026-09-01
Completion date
2026-12-31
Last updated
2025-09-17

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

Conditions

Coronary Artery Disease, Coronary Stenosis, Plaque, Atherosclerotic

Keywords

Coronary, Intravascular Imaging, Plaque

Brief summary

This investigation is to see if the new Novasight Hybrid imaging catheter can safely and accurately provide two different types of images (IVUS and OCT) of the inside of heart vessels at the same time. The images will be compared against one type of image (IVUS) to see if providing two, improves identification of different types of plaque (fatty substances) and informs better treatment. Atherosclerotic coronary artery disease is the name given to the development of plaques in the heart vessels. The plaques can cause narrowing in the vessels which may cause chest pain. Sometimes, plaques completely block the vessels causing a heart attack. This type of disease is the main cause of death worldwide. Research shows that when the type of plaque causing problems is known, it can help understanding of which narrowing may get worse and cause a heart attack. This information can also help with deciding when and which treatment to provide. Intravascular imaging is a way to assess the inside of the heart arteries. It involves passing a narrow catheter into the heart vessels. The catheter has a probe on its tip that emits light or an ultrasound signal. The signal is reflected by the vessel wall, back into the probe. A computer program interprets the signals and creates images of the inside of the arteries. There are two types of imaging catheters. One uses sound (Intravascular Ultrasound (IVUS)) and one uses light ((OCT) Optical Coherence Tomography) to produce different types of pictures of the vessels and plaques. The images produced by each type do not provide a full picture of the plaques on their own. A new hybrid imaging catheter has been developed which has two probes at the tip, an IVUS probe and an OCT probe and can produce both types of images at the same time. It is likely that having both types of images is better for finding high-risk plaques and should lead to better, more specific treatment. 50 heart attack patients who need an angiogram will have images of their vessels taken during their treatment. Once the imaging is complete the patient will continue with their routine planned care. The information from the images will be used to see how safe and accurate this new hybrid catheter is compared with the separate IVUS and OCT catheters, and also check to see if it is easier to identify plaques that might cause future problems. The study also aims to develop new ways to process and use the images from the hybrid catheter to better treat the plaques that cause the heart attack.

Interventions

DEVICEConavi Medical Novasight Hybrid System intervention

Patients for a coronary angiogram who meet the inclusion criteria and none of the exclusion criteria are enrolled. Participants are prepared for angiography and PCI procedure in the usual way. Radial or femoral artery cannulation is done under local anaesthetic and the angiogram performed as per standard practice. IVUS-OCT imaging of the culprit vessel using the Novasight Hybrid system is then performed. If image quality of the IVUS-OCT is suboptimal it will be repeated. If the IVUS-OCT catheter cannot cross the lesion, pre-dilatation is performed. The acquired IVUS-OCT images can be used to optimise PCI. Following PCI, angiography is repeated and if the findings are optimal, IVUS-OCT imaging is repeated. If the PCI results are suboptimal further stent optimisation is performed and IVUS-OCT imaging repeated; The procedure is then completed as clinically indicated. The participant will then receive conventional post PCI care

Sponsors

Rosetrees Trust
CollaboratorOTHER
National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
Conavi Medical Inc
CollaboratorUNKNOWN
Barts & The London NHS Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

A single-centre, prospective, non-randomized, open-label feasibility study of the Conavi Medical Novasight Hybrid System (IVUS and OCT) for stent optimization and atheroma assessment in patients who present with non-ST elevation myocardial infarction (NSTEMI).

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

General Inclusion Criteria 1. Age ≥ 18 to ≤80 years 2. Patient has capacity and willing to consent 3. Must be able to understand English language adequately 4. Patient admitted with an NSTEMI listed for coronary angiography Angiographic Inclusion Criteria 1) Culprit lesion amenable to PCI

Exclusion criteria

General

Design outcomes

Primary

MeasureTime frameDescription
To assess the superiority of IVUS-OCT over standalone IVUS in guiding PCIMeasured at procedureThe number of post PCI findings associated with worse outcomes (i.e., stent un-der expansion, major malappositions, major dissections, large thrombus burden and residual plaque at the edges of the stent) detected by the Conavi Medical Hybrid Imaging System and stand alone IVUS

Secondary

MeasureTime frameDescription
To examine the safety of the IVUS- OCT catheter in patients undergoing angiography and IVUS-OCT assessmentMeasured at procedure, at 1 week post procedure, at 1 month post procedure and 12 months post procedureThe number of device related complications (vessel perforation, dissection and acute vessel closure during or following IVUS-OCT imaging).
To examine the safety of the IVUS- OCT imaging procedureMeasured at procedure, at 1 week post procedure, at 1 month post procedure and 12 months post procedureThe number of procedural complications defined as: vessel perforation, angiographic dissection, stent thrombosis, thrombus embolization and acute vessel closure.
To examine the safety of the IVUS- OCT catheter in patients undergoing angiography and intravascular imagingMeasured at procedure, at 1 week post procedure, at 1 month post procedure and 12 months post procedureThe number of participant deaths or myocardial infarctions

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026