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Drug-Eluting Balloons vs Mimetic Stents for Popliteal Artery Disease

Comparative Study Between Drug-Eluting Balloons and Mimetic Stents for Popliteal Artery Disease Treatment in Patients With Chronic Lower Limb Ischemia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05651165
Enrollment
110
Registered
2022-12-14
Start date
2021-12-01
Completion date
2024-01-31
Last updated
2022-12-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Popliteal Arterial Stenosis

Keywords

Popliteal artery stenosis, Mimetic stent, Pharmacoactive balloon angioplasty, Chronic lower limb ischemia

Brief summary

More advanced and severe cases of chronic lower limb ischemia (the so-called critical lower limb ischemia) are painful and limiting conditions that impact on patients' quality of life. Until now, the available evidence for the femoropopliteal area only defines open surgery or endovascular treatment indications. However, the best strategy for endovascular procedures is still unclear. The popliteal artery is a challenging anatomical site for balloon angioplasty alone and standard nitinol stenting angioplasty. This randomized clinical trial aims to assess the superiority of nitinol stent angioplasty compared to pharmacoactive balloon angioplasty to treat critical lower limb ischemia due to popliteal artery arteriosclerosis.

Detailed description

Arteriosclerosis is a systemic and multi-etiological disease that causes arterial degeneration, narrowing their lumens and reducing perfusion in their respective territories. Chronic lower limb ischemia is one manifestation of arteriosclerosis. It may be initially asymptomatic, but patients usually present with pulselessness and intermittent lower limb claudication. More advanced and severe cases present with rest pain, the so-called critical lower limb ischemia. Critical lower limb ischemia usually benefits from revascularization and requires cautious surgical planning with complementary imaging tests able to locate the lesion site precisely. In our setting, the most used test is arterial cartography with doppler ultrasound. Afterward, surgeons should decide whether to perform open surgery or endovascular treatment. Until now, the available evidence for the femoropopliteal area only defines open surgery or endovascular treatment indications. However, the best strategy for endovascular procedures is still unclear. Given its anatomy, the popliteal artery undergoes many flexion-extension and rotational movements, making it a challenging site for balloon angioplasty alone (high incidence of restenosis) and standard nitinol stenting angioplasty (risk of stent fractures). Mimetic stents have been developed to overcome the risk of stent fractures. They consist of multiple intertwined nitinol wires that provide greater radial resistance and allow for even stress distribution. This randomized clinical trial aims to assess the superiority of nitinol stent angioplasty compared to pharmacoactive balloon angioplasty to treat critical lower limb ischemia due to popliteal artery arteriosclerosis.

Interventions

DEVICEPharmacoactive balloon angioplasty. Lutonix®

Percutaneous transluminal angioplasty with paclitaxel-coated balloon in the arteriosclerosis site to increase blood-flow to the distal arterial areas.

DEVICEMimetic stent.Supera®

Multiple intertwined nitinol wires that provide greater radial resistance and allow for even stress distribution. Implanted through percutaneous transluminal angioplasty in the arteriosclerosis site to increase blood-flow to the distal arterial areas.

Sponsors

Hospital Universitari de Bellvitge
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Open label, parallel-group, randomized (1:1) clinical trial.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients diagnosed of critical lower limb ischemia according to the TASC (TransAtlantic Inter-Society Consensus) working group. 2. Patients admitted to the Vascular Surgery Department of the Bellvitge Hospital University to treat critical lower limb ischemia for endovascular treatment. 3. With involvement of the Popliteal artery in-between the Hunter's canal and the start of the tibial artery branch. 4. WOCBP must use highly effective methods of contraception. 5. Patients who sign the written informed consent.

Exclusion criteria

1. Patients diagnosed of critical lower limb ischemia according to the TASC working group undergoing medical treatment or open surgery. 2. Patients requiring amputation. 3. Patients who underwent previous revascularization of the same limb (same artery). 4. The main involvement is from an arterial territory other than the popliteal artery. 5. Pregnant women. 6. Inability of overcoming the arterial lesion during the endovascular procedure. 7. Affected artery's diameter \<4 mm.

Design outcomes

Primary

MeasureTime frameDescription
Permeability12 monthsDegree of arterial permeability after intervention measured by arterial cartography with ultrasound at 3, 6 and 12 months.

Secondary

MeasureTime frameDescription
Limb salvage rate12 monthsNumber (percentage) of limbs that did not undergo further amputation.
Limb reintervention rate12 monthsNumber (percentage) of limbs that required reintervention.
Deaths12 monthsNumber (percentage) of deaths by any cause.

Countries

Spain

Contacts

Primary ContactCarlos M Rico, MD
carlosmartinezrico@gmail.com034 932 60 75 00
Backup ContactMalka Huici, MD
malkahuici@gmail.com034 932 60 75 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026