ATHERO: Advanced Technology Halting Early Re-Stenosis and Occlusion

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2006 by University of California, San Diego.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University of California, San Diego
ClinicalTrials.gov Identifier:
NCT00407940
First received: December 4, 2006
Last updated: NA
Last verified: December 2006
History: No changes posted
  Purpose

The rise of minimal access surgery has heralded the approval of a number of endovascular devices with similar indications. This is particularly true for the treatment of lower extremity ischemia. Comparable devices are selected for patient use somewhat arbitrarily, often dependent on industry influence. An unmet need is NON-industry sponsored prospective trials COMPARING devices head-to-head so that endovascular surgeons can even contemplate evidence-based device selection. At present, we seek to compare two new high-technology devices that are indicated to treat lower extremity arterial stenoses associated with claudication.


Condition Intervention Phase
Arterial Occlusive Disease
Intermittent Claudication
Device: Lower extremity Atherectomy and Cryoplasty
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: ATHERO: Advanced Technology Halting Early Re-Stenosis and Occlusion. A Prospective Randomized Trial Comparing Silverhawk™ Atherectomy to CryoPlasty® Therapy for Lower Extremity Claudication

Resource links provided by NLM:


Further study details as provided by University of California, San Diego:

Primary Outcome Measures:
  • Primary target patency at 12 months. The “target” is the index stenotic lesion(s). Primary patency is defined as <50% residual stenosis by duplex (color-flow Doppler) scan analysis, with antegrade flow to the target vessel.

Secondary Outcome Measures:
  • Ankle Brachial Index (ABI) improvement by ≥0.15 at 3, 6 and 12 months compared to baseline
  • Change in Walking Impairment Questionnaire (WIQ) functional status scores from baseline at 3, 6 and 12 months
  • Complications: defined as adverse events (AEs) or serious adverse events (SAEs). Complications may or may not be device related
  • Cost to patient and hospital: Including operating room times and duration of hospitalization.

Estimated Enrollment: 100
Study Start Date: December 2006
Estimated Study Completion Date: December 2008
Detailed Description:

Peripheral arterial disease affects more than 12 million Americans, and its incidence is growing annually. The male/female ratio of patients with claudication is just under 2/1. The arteries involved by atherosclerosis involve the arteries to the thigh and leg. These include the femoral and popliteal arteries. Fifty percent of people with femoral-popliteal PVD are symptomatic. Symptoms are typically related to exertional fatigue of thigh and calf muscles. These symptoms, referred to as claudication, seldom represent a life or even limb-threatening process. They do, however, result in significantly decreased productivity and an often devastating quality of life.

Traditional interventions for lower extremity claudication include technologies invented in the first half of the 20th century including surgical bypass; and those invented in the second half of the twentieth century, including balloon angioplasty and stenting. These interventions have substantial shortcomings. It is, however, relevant to note that endovascular (aka endoluminal or endovascular surgery) is becoming increasingly popular and gaining wide-spread support from vascular interventionalist societies wordwide.

The main shortcomings of angioplasty and stenting is the resultant inflammatory response. The mechanical injury to blood vessels is followed by a complex repair response comprising intimal vascular smooth muscle cell (VSMC) hyperplasia, vessel wall scarring and shrinkage of the vascular lumen, often resulting in reduced blood flow and subsequent muscle (or end organ) ischemia. Rodent, rabbit and large animal models have provided valuable insights into the pathophysiology of these responses.

The devices utilized in this protocol are both FDA approved for the procedures described in the protocol. The devices include the Silverhawk™ System (FoxHollow Technologies, Redwood City, CA) and the PolarCath™ Peripheral Dilatation System, Boston Scientific, Natick, Massachusetts). Hereafter both products will be referred to as the “Devices.”

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • The subject must give written informed consent and possess decision making capacity free of sedative or hypnotic agents.
  • Age 18 years or older
  • Candidate for angiography with intent-to-treat as determined by the Principle Investigator
  • On angiography, ipsilateral to a symptomatic limb, a stenotic or occluded de novo or restenotic lesion in the common femoral artery, superficial femoral artery or above the knee popliteal artery measuring no longer than 10 cm (the upper limit of treatment in Cryoplasty pre-marketing)
  • On angiography Lesion stenoses between 50% and 100% (inclusive)
  • At least one runoff vessel
  • Available for follow-up assessments

Exclusion Criteria:

  • Contraindication to systemic anticoagulation e.g. history of documented hemorrhage requiring treatment within the past 30 days; history of a hereditary bleeding disorder or known bleeding diathesis; major surgery or trauma, open chest massage, ocular surgery or hemorrhagic retinopathy within the past 30 days; puncture at a non-compressible site within 48 hours prior to planned procedure; history of stroke, intracranial hemorrhage, or central nervous system structural abnormalities within the past 3 months
  • History of endovascular surgery procedure or open vascular surgery on the index limb within the last 30 days
  • History of significant acute or chronic kidney disease that would preclude contrast angiography
  • Known allergy to contrast agents
  • History of heparin-induced thrombocytopenia (HIT)
  • Participation in any study of an investigational device, medication, biologic, or other agent within 30 days prior to randomization
  • Any thrombolytic therapy within 30 days of randomization
  • Pregnancy, lactation, or possession of any child bearing potential without evidence of surgical infertility or passage of 12 months since the last day of the subject’s last menstrual period.
  • Target lesion involving a dacron prosthesis or a prosthetic of unknown material
  • Target lesion extending into the orifice of the profunda femoris artery
  • Prisoner status
  • Any other subject feature that in the opinion of the investigator should preclude study participation
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00407940

Contacts
Contact: Joshua I Greenberg, MD 619-543-6222 jigreenberg@ucsd.edu
Contact: Ahmed Suliman, MD 619-543-6222 asuliman@ucsd.edu

Locations
United States, California
University of California, San Diego Medical Center, Hillcrest Recruiting
San Diego, California, United States, 92121
Contact: Joshua I Greenberg, MD    619-543-6222    jigreenberg@ucsd.edu   
Contact: Ahmed Suliman, MD    619-543-6222    asuliman@ucsd.edu   
Principal Investigator: Niren Angle, MD         
Sub-Investigator: Joshua I Greenberg, MD         
Sponsors and Collaborators
University of California, San Diego
Investigators
Principal Investigator: Niren Angle, MD University of California, San Diego
  More Information

Publications:
ClinicalTrials.gov Identifier: NCT00407940     History of Changes
Other Study ID Numbers: 007A
Study First Received: December 4, 2006
Last Updated: December 4, 2006
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, San Diego:
Thrombosis
Claudication

Additional relevant MeSH terms:
Intermittent Claudication
Arterial Occlusive Diseases
Arteriosclerosis
Vascular Diseases
Cardiovascular Diseases
Signs and Symptoms

ClinicalTrials.gov processed this record on September 22, 2014