Popliteal Artery Stenosis Clinical Trial
Official title:
DIRECTIONAL ATHERECTOMY WITH ANTIRESTENOTIC THERAPY vs PTA/SUPERA STENTING FOR POPLITEAL ARTERY ATHEROSCLEROTIC LESIONS: A CASE-MATCH PROPENSITY STUDY
NCT number | NCT05617053 |
Other study ID # | PI 22-2967 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 1, 2016 |
Est. completion date | October 1, 2022 |
The purpose of this study was to compare the results of directional atherectomy with antirestenotic therapy (DAART technique) and angioplasty/Supera stenting for the treatment of popliteal atherectomy lesions.
Status | Completed |
Enrollment | 143 |
Est. completion date | October 1, 2022 |
Est. primary completion date | January 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility | Inclusion Criteria: - patients with lifestyle limiting intermittent claudication ischemic rest pain, ischemic ulcers or gangrene (Rutherford class 3 to 6) who presented atherosclerotic lesions in the popliteal artery undergoing endovascular treatment by DAART of PTA/Supera stenting and at least a 12-months of follow-up Exclusion Criteria: - Exclusion criteria were patients who could not receive antiplatelet or anticoagulation therapies. Other exclusion criteria were patients with aneurysm of the ipsilateral superficial femoral artery or popliteal artery, acute thrombus, unsalvageable limb, very limited life-expectancy or with doubts in their willingness or capability to allow follow-up examinations. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Vascular Investigation Network Spanish Society for Angiology and Vascular Surgery |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Primary latency 12-months | primary patency at 12-months follow-up, defined as absence of binary restenosis or reocclusion on duplex ultrasound examination without repeat target lesion interventions | 12 months | |
Secondary | Secondary Patency | Secondary patency was defined as requiring a secondary intervention to restore patency after occlusion of the treated segment | 12-months | |
Secondary | Mortality | Patients dead all-cause during follow-up | 12-months | |
Secondary | Amputation rate | Patients with minor or mayor amputation during follow-up | 12-months | |
Secondary | Clinical status | Rutherford classification clinical scale after 12-month follow-up | 12-months | |
Secondary | ABI measurement | Ankle/Brachial index measurement. | 12-months | |
Secondary | Stent fracture | Stent fracture and implantation defects were assessed by high-resolution radiographic imaging performed on the stents of every limb | 12-months | |
Secondary | Primary-assisted patency | Primary assisted patency was defined as a patent popliteal segment that underwent further intervention within the inflow, treated vessel segment, or outflow of the treated vessel segment to improve patency | 12-months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01947478 -
MDT-2113 Drug-Eluting Balloon vs. Standard PTA for the Treatment of Atherosclerotic Lesions in the Superficial Femoral Artery and/or Proximal Popliteal Artery
|
N/A | |
Not yet recruiting |
NCT04175197 -
LegDeb2 Global Registry for Use of Legflow in Peripheral Arteries
|
||
Completed |
NCT01566461 -
IN.PACT Admiral Drug-Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Superficial Femoral Artery (SFA) and Proximal Popliteal Artery (PPA)
|
N/A | |
Completed |
NCT01412541 -
Moxy Drug Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Femoropopliteal Arteries
|
N/A | |
Not yet recruiting |
NCT06410313 -
First In Human Study to Assess Safety and Efficacy of the ChampioNIRâ„¢ Drug Eluting Peripheral Stent in the Treatment of Patients With Superficial Femoral Artery Disease and/or Proximal Popliteal Artery Disease
|
N/A | |
Recruiting |
NCT04709887 -
Appropriate Strategy of Surgical Treatment in Ischemic Diabetic Foot
|
N/A | |
Active, not recruiting |
NCT05734157 -
CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Proximal Popliteal Artery
|
N/A | |
Completed |
NCT05608655 -
DKutting Balloon Versus Chocolate Balloon to Treat Femoral and Popliteal Artery Stenosis
|
N/A | |
Withdrawn |
NCT04700371 -
Vessel Deformations and Restenosis After Stenting of the Popliteal Artery
|
N/A | |
Terminated |
NCT02813577 -
Lutonix Drug Coated Balloon for Treatment of Femoropopliteal Arteries in United States Females (CONFIRM)
|
N/A | |
Completed |
NCT03844724 -
Drug-eluting PTA Balloon Dilatation Catheter in the Treatment of Peripheral Artery Stenosis or Occlusion
|
N/A | |
Recruiting |
NCT06416644 -
The PORTuguese Registry of Supera Supported Femoral-Fopliteal Revascularization (SupPORT Registry)
|
N/A |