Clinical Trials Logo
  1. Home
  2. Other
  3. NCT01602159

Revascularization With Open Bypass Versus Angioplasty and STenting of the Lower Extremity Trial (ROBUST) — ROBUST  

Claudication Clinical Trial

Official title:
Revascularization With Open Bypass Versus Angioplasty and STenting of the Lower Extremity Trial (ROBUST)

Clinical Trial Summary

This is a prospective randomized controlled trial to compare clinical improvement, cost effectiveness and patency rates between new and improved Nitinol stents and open bypass surgery in the superficial femoral artery disease.

Secondary outcomes also include comparing quality of life, re-intervention rate, mortality, morbidity and time to return to work or regular activities.

Patients with superficial femoral artery lesions will be considered. Patients with TASC II A lesions will not be randomized but treated with PTA/stenting as standard of care. Patients with TASC II B and C lesions will be prospectively randomized into either receiving open bypass or stenting.

Patients with TASC D lesions will be treated with open bypass surgery after angiography.

The investigators will collect pre-procedure, peri-procedural and clinical follow-up data on all enrolled the patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01602159
Study type Interventional
Source Johns Hopkins University
Contact
Status Completed
Phase N/A
Start date July 2009
Completion date June 2014
View Details
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05712395 - The Effects of a Novel, Non-ischemic and Pain-free Exercise Intervention in Peripheral Artery Disease N/A
Completed NCT01359423 - Comparison of Primary Long Full Coverage Stenting vs Primary Short Spot Stenting for Long Femoropopliteal Artery Disease. N/A
Recruiting NCT02389023 - Comparison of Prevena Negative Pressure Incision Management System vs. Standard Dressing After Vascular Surgery N/A
Completed NCT00962897 - Comparison of Prosthetic Femoropopliteal Bypass Versus Viabahn Endoprosthesis for Treatment of Symptomatic Femoral Artery Occlusion N/A
Completed NCT00693823 - Comparison of Prosthetic Femoropopliteal Bypass Versus Viabahn Endoprosthesis for Treatment of Symptomatic Femoral Artery Occlusive Disease N/A
Completed NCT02475200 - Phoenix Post-Approval Registry - Using the Phoenix Atherectomy Systems
Completed NCT03288181 - Effects of Passive Muscle Stretching on Vascular Function and Symptoms of PAD N/A
Recruiting NCT01450722 - Paclitaxel Eluting Stent in Long SFA Obstruction: A Prospective, Randomized Comparison With Bypass Surgery Phase 3
Completed NCT01734603 - Intensive Rehabilitation in Peripheral Arterial Disease With Claudication: Effects of a Treadmill Training With Active Recovery Phase 3
Recruiting NCT01231360 - The Effect of Exercise Training on Skeletal Muscle Metabolism in Peripheral Artery Disease (PAD) N/A
Terminated NCT01022606 - Intra-arterial Measurement of pO2 in Walking Induced Transient Hack Profiles Phase 1
Active, not recruiting NCT00390767 - Safety Study of MultiGeneAngio in Patients With Peripheral Arterial Disease (PAD) Phase 1/Phase 2
Terminated NCT01808989 - Clinical Interest of the TcPO2 Technique
Completed NCT01858363 - ILLUMENATE EU Randomized Clinical Trial N/A
Terminated NCT01341340 - The ABSORB BTK (Below The Knee) Clinical Investigation N/A
Completed NCT01468974 - ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbable Vascular Scaffold) System N/A
Completed NCT02341664 - Patient and Provider Assessment of Lipid Management Registry
Completed NCT04058171 - Validation of a Treadmill Walking Test to Discriminate Neurogenic Claudication From Vascular Claudication
Completed NCT02719665 - THE OMEGA-SPM-DOSE and OMEGA-SPM-PAD: Specialized Pro-Resolving Mediators in Patients With Peripheral Artery Disease N/A
Not yet recruiting NCT03845036 - The Effects of Diet and Exercise Interventions in Peripheral Artery Disease N/A