Peripheral Artery Disease Clinical Trial
— OPTIMISEOfficial title:
Optical Imaging Measurement of Intravascular Solution Efficacy Trial
NCT number | NCT01743872 |
Other study ID # | OPTIMISE |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2012 |
Est. completion date | June 2016 |
Verified date | August 2022 |
Source | University Hospitals Cleveland Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Iodinated contrast is the current gold standard for infrainguinal angiography imaging in patients without renal insufficiency and has also been used with intravascular Optical Coherence Tomography (iOCT) to improve image quality in human coronary arteries as well as carotid arteries. The current debate in the literature for iOCT medium is between iodinated contrast and dextran and CO2 may offer a superior method of iOCT imaging during lower extremity occlusive disease interventions. The investigators hypothesize that the CO2 medium injection during iOCT data acquisition is feasible and will produce at least the same quality of imaging as that obtained with contrast or dextran without causing the problems of volume overload and renal toxicity seen with the two latter mediums. Primary Outcomes Measured - Quality: Cumulative number of clear image frame (CIF) through the entire 54mm length segment. - Quantitative: Calculations of the area and diameter of each segment will be measured to determine if index of refraction has any effect between the three mediums to be tested. The investigators expect to find little difference between all three iOCT mediums and hope to conclude that CO2 offers a superior side effect profile for iOCT imaging in the lower extremity arterial system.
Status | Completed |
Enrollment | 23 |
Est. completion date | June 2016 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | University Hospitals Case Medical Center | Cleveland | Ohio |
Lead Sponsor | Collaborator |
---|---|
University Hospitals Cleveland Medical Center |
United States,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Quality of Images | The metric of image quality was the clear imaging field (CIF), which was defined as a cross section in which =270° of the vessel wall architecture was visualized. This has been used previously to quantify adequacy of clearance in OCT image comparison. Two independent observers, blinded to the flush medium used, analyzed all OCT frames in each pullback sequence. Any disagreement >10% was resolved with a consensus re-evaluation at a later time point by the same reviewers. Each individual cross section was assigned a designation of quality or insufficient quality; thus, a quality image proportion was generated for each run by taking the mean of each observer's determinations | 1 month | |
Secondary | Superficial Femoral Artery Plaque Composition by Flush Medium | 1 month |
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