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Study Comparing Two Methods of Expanding Stents Placed in Legs of Diabetics With Peripheral Vascular Disease (COBRA)
This study is currently recruiting participants.
Study NCT00827853   Information provided by North Texas Veterans' Healthcare System
First Received: January 22, 2009   No Changes Posted
This Tabular View shows the required WHO registration data elements as marked by

January 22, 2009
January 22, 2009
November 2008
Rate of binary restenosis as determined by duplex ultrasound. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Same as current
No Changes Posted
Resting ankle-brachial index [ Time Frame: 6 months and 1 year ] [ Designated as safety issue: No ]
Same as current
 
Study Comparing Two Methods of Expanding Stents Placed in Legs of Diabetics With Peripheral Vascular Disease
PolarCath® Cryoplasty Versus Conventional Balloon Post-Dilation of Nitinol Stents for Peripheral Vascular Interventions (COBRA)

Despite recent advances in stent technology and its widespread application in the treatment of peripheral vascular disease (PVD), incidences of partial or complete blockage of stent lumen (in-stent restenosis) due to in growth of cells (neo-intimal proliferation) is unacceptably high.

In diabetics with long superficial femoral artery (SFA) lesions, in-stent restenosis rates are higher than in non-diabetics. Consequently interventional techniques that curtail in-stent restenosis have to be explored. Cryoplasty is a stent expansion method in which a balloon is expanded using pressurized nitrous oxide gas. As the nitrous oxide expands in the balloon it cools the surroundings to about -10 degrees C. This induces programed death (apoptosis) of the smooth muscle cells in arterial wall.

The investigators hypothesize that Cryoplasty, by inducing an apoptotic smooth muscle cell response, when applied to post-dilation of nitinol self-expanding stents in the Superficial Femoral Artery (SFA) of diabetics, would lead to decreased in-stent restenosis due to decreased neointimal proliferation.

The pre-recruitment process would identify diabetics who have life-style limiting claudication in their legs. Based on the physicians decision such patients may have to undergo a peripheral vascular intervention of the SFA, with placement of self-expanding nitinol stents. If such a decision is made, the patient will be randomized to either cryoplasty balloon post-dilation of the stent or to conventional angioplasty balloon post-dilation after obtaining informed consent. At one year, in segment (stent + 10 mm beyond its proximal and distal edges) peak systolic velocity by duplex ultrasound will be measured in all subjects to assess the rate of binary resteosis defined as a > or = 2.5 times increase in peak systolic velocity (primary endpoint). A 6 month resting ankle brachial index, and binary restenosis may be assessed as a secondary endpoint of the study.

 
Interventional
Treatment, Randomized, Single Blind (Subject), Parallel Assignment, Efficacy Study
Peripheral Vascular Disease
  • Procedure: Conventional angioplasty balloon
  • Procedure: cryoplasty balloon
  • Experimental: Conventional angioplasty balloon post-dilation
  • Experimental: Cryoplasty balloon post-dilation

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
132
December 2010
November 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Diabetics, insulin or non-insulin dependent above 21 years of age
  • Able to provide an informed consent
  • Life expectancy > 1 year
  • Presenting with with moderate claudication (Rutherford stage 2), severe intermittent claudication (Rutherford stage 3), chronic critical limb ischemia with pain while the patient was at rest(Rutherford stage 4), or chronic critical limb ischemia with ischemic ulcers/gangrene(Rutherford stage 5/6)
  • Placement of > 5 mm in diameter self-expanding Nitinol stent in the SFA, with at least 1 vessel infra-popliteal runoff
  • Placement of > 60 mm in length self-expanding Nitinol stent in the SFA, with at least 1 vessel infra-popliteal runoff

Exclusion Criteria:

  • Serum creatinine of >= 2.0 mg/dl
  • Presence of iodinated contrast allergy
  • Presence of allergy to Aspirin and Plavix
  • Pregnancy
  • Relative or absolute contraindication for anticoagulation
  • History of allergy to Angiomax and unfractionated heparin or heparin induced thrombocytopenia (HIT)
  • White blood count < 3000; platelet count < 100000, and baseline hemoglobin < 10 g/dl
  • Absence of brisk at least 1 vessel infra-popliteal runoff to the foot
  • Left ventricular ejection fraction < 25%
  • Relative or absolute contraindication for anticoagulation
Both
21 Years and older
No
Contact: Subhash Banerjee, MD (214)857-1608 subhash.banerjee@utsouthwestern.edu
Contact: Cyril Varghese, MS zcman84@yahoo.com
United States
 
 
NCT00827853
Dr. Subhash Banerjee, Acting chief of cardiology, Dallas Veterans Hospital
 
Boston Scientific Corporation
Texas Health Resources
Principal Investigator: Subhash Banerjee, MD VA North Texas Healthcare Systen, Dallas, TX
Study Director: Emmanouil S Brilakis, MD, PhD VA North Texas Healtcare System, Dallas, TX
Study Director: Tony S Das, MD Texas Health Resources
North Texas Veterans' Healthcare System
January 2009

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.