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EXCImer Laser Randomized Controlled Study for Treatment of FemoropopliTEal In-Stent Restenosis
The purpose of the study is to evaluate the safety and efficacy of laser atherectomy with balloon angioplasty compared to balloon angioplasty alone in the treatment of above the knee peripheral artery in-stent restenosis.
Age
18 - 85 years
Sex
ALL
Healthy Volunteers
No
St. Vincent's East
Birmingham, Alabama, United States
Thomas Hospital
Fairhope, Alabama, United States
St. Vincent Heart Clinic Arkansas
Little Rock, Arkansas, United States
Arkansas Heart Hospital
Little Rock, Arkansas, United States
UC-Davis Medical Centers
Sacramento, California, United States
Yale - New Haven Hospital
New Haven, Connecticut, United States
Washington Hospital Center
Washington D.C., District of Columbia, United States
The Cardiac and Vascular Institute
Gainesville, Florida, United States
Memorial Regional Hospital
Hollywood, Florida, United States
Mount Sinai Medical Center
Miami, Florida, United States
Start Date
June 1, 2011
Primary Completion Date
March 1, 2014
Completion Date
May 1, 2015
Last Updated
August 18, 2016
252
ACTUAL participants
Turbo Elite Laser and Turbo Tandem Laser Guide Catheters
DEVICE
Balloon angioplasty
PROCEDURE
Lead Sponsor
Spectranetics Corporation
NCT07472049
NCT07161583
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07322913