Scientific Proposal to Substantiate Vascular Effects Through Sirolimus vs. Paclitaxel DCB Implantation

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Endovascular treatment of symptomatic atherosclerotic peripheral artery disease (PAD) is recommended as the primary revascularization strategy. Percutaneous transluminal angioplasty (PTA) of the superficial femoral artery has a high initial success rate, but restenosis and dissections frequently occur.The influence of the novel devices with improved hemodynamic capabilities with respect to vasomotion of the vessel wall, vascular function and vascular compliance can be measured by FMD (flow-mediated dilation), arterial stiffness indices and vascular strain analysis. The aim of this ITT is to determine the potential improvement and impact of the SELUTION SLR in the infrainguinal arteries on local vascular function.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Peripheral artery disease

• Target lesions 3 cm distal to the CFA-bifurcation including SFA and PA lesions

• Clinical diagnosis of chronic, symptomatic lower limb ischemia as defined by Rutherford 2, 3, 4 and 5

• Planed peripheral intervention TASC A-D

• Subject must be between 18 and 85 years old

• Female of childbearing potential must have a negative pregnancy test within 10 days prior to index procedure and utilize reliable birth control until completion of the 12-month angiographic evaluation

• Vessel diameter ≥4.0 mm and ≤7.0 mm

• Willing to comply with the specified follow-up evaluation

• Written informed consent prior to any study procedures

• Pretreatment with an adequately sized balloon

Locations
Other Locations
Germany
University of Essen, Clinic of Cardiology and Angiology
RECRUITING
Essen
Contact Information
Primary
Christos Rammos, Professor
christos.rammos@uk-essen.de
0201-723-84808
Backup
Tienush Rassaf, Univ.-Prof.
tienush.rassaf@uk-essen.de
0201-723-4801
Time Frame
Start Date: 2022-04-06
Estimated Completion Date: 2024-04-06
Participants
Target number of participants: 70
Treatments
Experimental: SELUTION SLR DCB
Sustained Limus Release drug eluting balloon
Active_comparator: Paclitaxel eluting balloon
Conventional: Medtronic INpact
Sponsors
Leads: University Hospital, Essen

This content was sourced from clinicaltrials.gov