Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusive Disease

NAWithdrawnINTERVENTIONAL
0
Timeline

Start Date

December 1, 2017

Primary Completion Date

December 1, 2017

Study Completion Date

December 1, 2017

Conditions
Femoropopliteal Stenosis
Interventions
DEVICE

Supera Stent

Angioplasty and stenting will performed according to the guidelines of the Society of Interventional Radiology and the instruction for use for each stent. Patients will be allocated to Supera stent versus LifeStent based on block randomization (block size 4 patients).

DEVICE

Life Stent

Angioplasty and stenting will performed according to the guidelines of the Society of Interventional Radiology and the instruction for use for each stent. Patients will be allocated to Supera stent versus LifeStent based on block randomization (block size 4 patients).

Trial Locations (2)

B3H 2Y9

Queen Elizabeth II Health Sciences Centre, Halifax

H2L 4M1

Centre hospitalier de l'université de Montréal, Montreal

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Abbott Medical Devices

INDUSTRY

collaborator

Centre de Recherche du Centre Hospitalier de l'Université de Montréal

OTHER

collaborator

Queen Elizabeth II Health Sciences Centre

OTHER

lead

Centre hospitalier de l'Université de Montréal (CHUM)

OTHER