Carotid Stenosis Clinical Trial
Official title:
3D Interventional Tools for Endovascular Procedures in the OR
Verified date | March 2022 |
Source | Philips Clinical & Medical Affairs Global |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
As endovascular procedures become more complex, there is a growing need for 3D image overlay to assist with device guidance and placement. Currently, a 3D image is typically created intra-operatively using 3D rotational angiography (3D-RA) or cone-beam CT (XperCT). This 3D image may then be overlaid on live fluoroscopy to provide 3D guidance information (Dynamic 3D Roadmapping). Philips Healthcare multimodality overlay products allows registration of a pre-acquired MR/CT or 3D rotational image to live fluoroscopy.
Status | Completed |
Enrollment | 58 |
Est. completion date | August 1, 2021 |
Est. primary completion date | April 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: - Patients with age 18-90, of both genders and all races - Patients undergoing elective AAA or TAA repair or carotid stenting or peripheral intervention - Patients already selected for endovascular treatment by preoperative CT angiogram - Patients with preoperative CT performed within 4 months of operation Exclusion Criteria: - Patients refusing or incapable of providing informed consent - Patients undergoing emergent or ruptured AAA repair - Patients with known connective tissue disorders - Patients with aortic dissections - Patients participating in other EVAR, IDE, or IND trials - Patients with anticipated adjunctive intervention requiring additional intravenous contrast - Patients with anticipated endograft extension distal to the common iliac artery - Patients without CT angiogram performed at BIDMC with standard EVAR protocol - Patients without CT angiogram performed within 4 months of operation - Patients with glomerular filtration rate (GFR) < 60 mL/min/1.73m2 - Patients with contraindication to intravenous contrast - Patients with disability or previous implants precluding adequate visualization on rotational imaging |
Country | Name | City | State |
---|---|---|---|
United States | Beth Israel Deaconess Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Philips Clinical & Medical Affairs Global |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | feedback to improve the usability of the Vessel Navigator | PI answers questions to help improve the usability of the VesselNavigator | one month after procedure |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03631381 -
Retrospective Study of Carotid Surgery in Dijon
|
||
Completed |
NCT05437991 -
Ultrasonographic Morphology Assessment of Low-grade Carotid Stenosis
|
N/A | |
Completed |
NCT02722720 -
Carotid Arteries Stenting Complications: Transradial Approach Versus Transfemoral
|
N/A | |
Completed |
NCT02336958 -
Ultrasound Guided Intermediate Cervical Plexus Block and Additional Perivascular Local Anesthetic Infiltration
|
N/A | |
Completed |
NCT02630862 -
Oxidative Stress and Oxysterols Profiling in Patients With Carotid Revascularization
|
N/A | |
Completed |
NCT00536796 -
Percentage of Secondary Prevention Patients Treated to Their LDL-C Targets
|
N/A | |
Recruiting |
NCT05566301 -
Multicentric Study on Clopidogrel Resistance in DAPT for CAS (MULTI-RESCLOSA)
|
||
Completed |
NCT03303534 -
Short-Term Endogenous Hydrogen Sulfide Upregulation
|
N/A | |
Recruiting |
NCT05250349 -
TRAnscranial Doppler CErebral Blood Flow and Cognitive IMPAIRment in Heart Failure
|
||
Recruiting |
NCT05845710 -
Direct Access Carotid Artery Stenting Using the Neuroguard IEP System (PERFORMANCE III)
|
N/A | |
Recruiting |
NCT01732523 -
Predictive Value of Neovascularization Within Asymptomatic Carotis Stenosis on CEUS
|
||
Completed |
NCT01315288 -
A Randomized Trial of Clinical Decision Making in Asymptomatic Carotid Stenosis
|
N/A | |
Withdrawn |
NCT00401921 -
A Study of the Effects of Minocycline on Cognitive Function After Carotid Endarterectomy
|
Phase 2 | |
Recruiting |
NCT01273350 -
A Prospective, Non-Randomized, Evaluation of Low-Risk Patients Undergoing Carotid Stenting With ANgiomax (Bivalirudin)
|
N/A | |
Completed |
NCT03215563 -
PET-MRI Imaging in Patients With Acute Neurovascular Syndrome
|
||
Completed |
NCT03215550 -
PET-MRI Imaging in Patients With Symptomatic Carotid Artery Stenosis
|
||
Completed |
NCT04553549 -
Safety and Feasibility of the Infinity Catheter for Radial Access
|
||
Completed |
NCT03596229 -
Major Adverse Cardiac Events After Carotid Endarterectomy
|
||
Completed |
NCT04255316 -
Modified Method of Eversion Carotid Endarterectomy in Patients With Extensive Atherosclerotic Disease of Carotid Bifurcation
|
N/A | |
Completed |
NCT03410576 -
Perioperative Time Course of MMP-9 and Its Inhibitor During Carotid Artery Stenting and Carotid Endarterectomy
|
N/A |