Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Ischemia

N/ACompletedNCT02060630

Carelon Research1,843 enrolled

Overview

This study will compare the effectiveness of best available surgical treatment with best available endovascular treatment in adults with critical limb ischemia (CLI) who are eligible for both treatment options.

Male and female subjects aged 18 years or older will be randomized to receive either open surgical treatment or endovascular treatment. They will be followed for at least 2 years and up to 4 years and 2 months after treatment to primarily assess survival and major adverse limb events in the index or treated limb, and secondarily, to determine clinical and cost effectiveness outcomes after treatment. These outcomes (survival-free of major limb events and clinical, functional and cost effectiveness) will be compared within two cohorts of subjects: those with an available single-segment great saphenous vein, and those with an alternative conduit. The null hypotheses for both cohorts is that there will be no difference in MALE-free survival between best endovascular therapy and best surgical therapy.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

1,843

Conditions

Critical Limb Ischemia

Interventions

Open surgical revascularizationPROCEDURE

Endovascular revascularizationDEVICE

A variety of FDA approved devices will be used within this treatment arm. The trial will submit a proof-of-concept IDE application to the FDA to cover all devices.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Male or female, age 18 years or older. 2. Infrainguinal PAOD (occlusive disease of the arteries below the inguinal ligament). 3. CLI, defined as arterial insufficiency with gangrene, non-healing ischemic ulcer, or rest pain consistent with Rutherford categories 4-6. 4. Candidate for both endovascular and open infrainguinal revascularization as judged by the treating investigators 5. Adequate aortoiliac inflow. 6. Adequate popliteal, tibial or pedal revascularization target defined as an infrainguinal arterial segment distal to the area of stenosis/occlusion which can support a distal anastomosis of a surgical bypass. 7. Willingness to comply with protocol, attend follow-up appointments, complete all study assessments, and provide written informed consent. Exclusion Criteria: 1. Presence of a popliteal aneurysm (\>2 cm) in the index limb. 2. Life expectancy of less than 2 years due to reasons other than PAOD. 3. Excessive risk for surgical bypass (as determined by the operating surgeon and the CLI Team) 4. Planned above ankle amputation on ipsilateral limb within 4 weeks of index procedure. 5. Active vasculitis, Buerger's disease, or acute limb-threatening ischemia 6. Any prior index limb infrainguinal stenting or stent grafting associated with significant restenosis within 1 cm of stent or stent-graft, unless the occlusion/restenosis site is outside the intended treatment zone (i.e.,. a tibial vessel that is not currently intended to be revascularized as a part of the treatment for CLI). 7. Any of the following procedures performed on the index limb within 3 months prior to enrollment: 1. Infrainguinal balloon angioplasty, atherectomy, stent, or stentgraft; 2. Infrainguinal bypass with either venous or prosthetic conduit 8. Open surgical inflow procedure (aortofemoral, axillofemoral, iliofemoral, thoracofemoral or femorofemoral bypass) within 6 weeks prior to enrollment 9. Current chemotherapy or radiation therapy. 10. Absolute contraindication to iodinated contrast due to prior near-fatal anaphylactoid reaction (laryngospasm, bronchospasm, cardiorespiratory collapse, or equivalent) which would preclude patient participation in angiographic procedures. 11. Pregnancy or lactation. 12. Administration of an investigational drug for PAD within 30 days of randomization. 13. Participation in a clinical trial (except observational studies) within the previous 30 days. 14. Prior enrollment or randomization into BEST-CLI.

Locations (161)

Outcomes

Primary Outcomes

The primary efficacy endpoint: MALE (Major Adverse Limb Event)-free survival. MALE is defined as above ankle amputation of the index limb or major re-intervention (e.g. new bypass graft, jump/interposition graft revision, or thrombectomy/ thrombolysis)

* Time to major adverse limb event or death, whichever occurs first in subjects with Single-Segment Great Saphenous Vein (SSGSV) available * Time to major adverse limb event or death, whichever occurs first in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Secondary Outcomes

Clinical: Re-intervention and amputation-free survival (cohort 1)

Time to re-intervention of the index leg, above ankle amputation of the index leg, or death, whichever occurs first in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Re-intervention and amputation-free survival (cohort 2)

Time to re-intervention of the index leg, above ankle amputation of the index leg, or death, whichever occurs first in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from MALE-POD (POD, defined as death within 30 days of index procedure) (cohort 1)

Time to re-intervention of the index leg, amputation of the index leg, or death within 30 days of index procedure, whichever occurs first in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Clinical: Freedom from MALE-POD (POD, defined as death within 30 days of index procedure) (cohort 2)

Data from ClinicalTrials.gov

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The University of Alabama at Birmingham

Birmingham, Alabama, United States

Arizona Heart Hospital

Phoenix, Arizona, United States

University of Arizona - Banner University Medical Center

Tucson, Arizona, United States

Carondelet Heart & Vascular Institute

Tucson, Arizona, United States

University of Arkansas for Medical Services

Little Rock, Arkansas, United States

University of California - Irvine

Irvine, California, United States

San Diego VAMC

La Jolla, California, United States

UC San Diego Sulpizio Cardiovascular Center

La Jolla, California, United States

Loma Linda University Medical Center

Loma Linda, California, United States

Loma Linda VA Medical Center

Loma Linda, California, United States

...and 151 more locations

Time to re-intervention of the index leg, amputation of the index leg, or death within 30 days of index procedure, whichever occurs first in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Amputation-free survival (cohort 1)

Time to amputation of the index leg, or death, whichever occurs first in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Amputation-free survival (cohort 2)

Time to amputation of the index leg, or death, whichever occurs first in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from POD (POD, defined as death within 30 days of index procedure) (cohort 1)

Time to death within 30 days of index procedure in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom POD (POD, defined as death within 30 days of index procedure) (cohort 2)

Time to death within 30 days of index procedure in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from Myocardial Infarction (cohort 1)

Time to myocardial infarction (MI) in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from Myocardial Infarction (cohort 2)

Time to myocardial infarction (MI) in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from Stroke (cohort 1)

Time to stroke in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from Stroke (cohort 2)

Time to stroke in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from re-intervention (major and minor) in index leg (cohort 1)

Time to re-intervention (major and minor) in index leg in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from re-intervention (major and minor) in index leg (cohort 2)

Time to re-intervention (major and minor) in index leg in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Number of re-interventions (major and minor) in per limb salvaged (cohort 1)

Number of re-interventions (major and minor) in per limb salvaged in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Number of re-interventions (major and minor) in per limb salvaged (cohort 2)

Number of re-interventions (major and minor) in per limb salvaged in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from hemodynamic failure (cohort 1)

Time to hemodynamic failure in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from hemodynamic failure (cohort 2)

Time to hemodynamic failure in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from clinical failure (cohort 1)

Time to above ankle amputation, major reintervention, MALE, degradation of WIfI stage or death, whichever occurs first in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from clinical failure (cohort 2)

Time to above ankle amputation, major reintervention, MALE, degradation of WIfI stage or death, whichever occurs first in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from Critical Limb Ischemia (CLI) (cohort 1)

Time to resolution of presenting CLI symptoms in the index limb in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from Critical Limb Ischemia (CLI) (cohort 2)

Time to resolution of presenting CLI symptoms in the index limb in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from all-cause mortality (cohort 1)

Time to all-cause mortality in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Clinical: Freedom from all-cause mortality (cohort 2)

Time to all-cause mortality in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Quality of Life assessment using VasuQoL (cohort 1)

VasuQOL measurements in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Quality of Life assessment using VasuQoL (cohort 2)

VasuQOL measurements in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Quality of Life assessment using EuroQoL (cohort 1)

EuroQOL measurements in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Quality of Life assessment using EuroQoL (cohort 2)

EuroQOL measurements in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Function assessment using SF-12, PCS (cohort 1)

Physical Component Summary (PCS) scores in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Function assessment using SF-12, PCS (cohort 2)

Physical Component Summary (PCS) scores in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Function assessment using SF-12, MCS (cohort 1)

Mental Component Summary (MCS) scores in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Function assessment using SF-12, MCS (cohort 2)

Mental Component Summary (MCS) scores in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Function assessment using SF-12, SF-6D R2 (cohort 1)

Utility Index (SF-6D R2) scores in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Function assessment using SF-12, SF-6D R2(cohort 2)

Utility Index (SF-6D R2) scores in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Pain Now (cohort 1)

Scores for Pain Now in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Pain Now (cohort 2)

Scores for Pain Now in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Usual level of Pain (cohort 1)

Scores for Usual level of Pain during the last week in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Usual level of Pain (cohort 2)

Scores for Usual level of Pain during the last week in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Best level of Pain (cohort 1)

Scores for Best level of Pain during the last week in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Best level of Pain (cohort 2)

Scores for Best level of Pain during the last week in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Worst level of Pain (cohort 1)

Scores for Worst level of Pain during the last week in subjects with SSGSV available

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Functional: Numerical rating scale for Pain, Worst level of Pain (cohort 2)

Scores for Worst level of Pain during the last week in subjects without available SSGSV

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Function: Six-minute walk test (cohort 1)

Six-minute walk test measurements in subjects with SSGSV available. The six-minute walk test was performed at a subset of clinical sites (for whom this test was standard of care) and was limited to patients for whom rest pain, wounds, or foot surgery (recent or anticipated) did not preclude weight bearing

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject

Function: Six-minute walk test (cohort 2)

Six-minute walk test measurements in subjects without available SSGSV. The six-minute walk test was performed at a subset of clinical sites (for whom this test was standard of care) and was limited to patients for whom rest pain, wounds, or foot surgery (recent or anticipated) did not preclude weight bearing

Time frame: Through each subject's last regularly scheduled study visit, up to a maximum of 84 months per subject