Optical Imaging Measurement of Intravascular Solution Efficacy Trial (OPTIMISE)
Peripheral Artery Disease
About this trial
This is an interventional diagnostic trial for Peripheral Artery Disease focused on measuring Optical Coherence Tomography, Contrast, Dextran, Carbon Dioxide, Imaging, Catheter, Lower Extremity Artery
Eligibility Criteria
Inclusion Criteria:
- Age greater than or equal to 18 years
- English speaking
- Scheduled to undergo an infrainguinal angiogram and/or endovascular procedure as determined by a vascular surgery specialist
- Superficial Femoral Artery diseased segment
Exclusion Criteria:
- Acute or Chronic Renal insufficiency with Cr >1.5
- Chronic obstructive pulmonary disease
- Congestive heart failure (American Heart Association C lass III or IV)
- Acute limb ischemia, defined by a significant change in symptoms (one category on the Rutherford scale within the previous 14 days)
- Concurrent oral anticoagulant therapy that cannot be safely withheld
Sites / Locations
- University Hospitals Case Medical Center
Arms of the Study
Arm 1
Experimental
iOCT
Arterial access will performed by the operating surgeon. An aortic and infrainguinal angiogram using the standard method of intravenous iodinated contrast under digital subtraction fluoroscopy will be conducted in the usual manner according to the vascular surgeon. A 54 mm section of Superficial Femoral Artery will be chosen for study imaging. An intervention sheath or injection catheter will be placed just proximal to the area of interest. An 0.014" wire will be passed distal to the area of interest. The patient will then undergo OCT of this 54mm section with each of the three mediums below using a continuous flushing method through injection catheter. All OCT imaging will be collected at a rate of 25mm/sec. In the event of a subsequent procedure, OCT imaging will again be performed