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Trial record 3 of 8 for:    2004-06

Efficacy of Automated Distal Vascular Anastomosis in Coronary Surgery: Phase II

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00292500
Recruitment Status : Terminated (Cardica has terminated the development of the product for Business Reason.)
First Posted : February 16, 2006
Last Update Posted : August 21, 2013
Information provided by (Responsible Party):
Cardica, Inc

Brief Summary:
This evaluation is designed to evaluate the feasibility of using an automated distal coronary anastomotic to facilitate grafting of the left internal mammary artery to the left anterio descending coronary artery during myocardial revascularization in patients with coronary artery disease requiring surgical intervention. The study is designed to assess the ability to compare the patency of grafts created using an automated device versus hand-sewn grafts of the same vessels in the same patient population.

Condition or disease Intervention/treatment Phase
Coronary Artery Disease Device: Automated distal anastomotic device Not Applicable

Detailed Description:
Evaluation of automated distal anastomotic device as a surrogate for hand-sewn grafts for completion of arterial conduit anastomosis between the Left Internal Mammary Artery and Left Anterior Descending Artery among patients with coronary artery disease requiring surgical revascularization.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 170 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Efficacy of Automated Distal Vascular Anastomosis in Coronary Surgery: Phase II
Study Start Date : January 2006
Actual Primary Completion Date : October 2008
Actual Study Completion Date : December 2009

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
No Intervention: C-Port
Automated distal anastomotic device
Device: Automated distal anastomotic device
Other Name: C-Port xA Distal Anastomosis System

Primary Outcome Measures :
  1. Coronary patency of index graft at the sixth post-operative month [ Time Frame: 6 months post-op ]

Secondary Outcome Measures :
  1. Establish preliminary safety profile [ Time Frame: 6 months post-op ]

Information from the National Library of Medicine

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, Learn About Clinical Studies.

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Ages Eligible for Study:   50 Years to 85 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Age between 50 and 85 years (inclusive)
  • Diagnostically confirmed coronary disease
  • Ejection fraction > 30%
  • Tolerate contrast media
  • Acceptable LIMA (conduit) and LAD (target)for grafting
  • Life expectancy > 1 year

Exclusion Criteria:

  • Refusal to give informed consent
  • Unable to meet study travel and general health requirements
  • Pregnancy
  • Previous cardiac surgery
  • NYHA Class IV
  • Preoperative need for IABP
  • Acute or chronic dialysis (creatinine > 200mmolor 2.3 mg/dL) within 30 days of surgery
  • Acute or suspected systemic infection
  • Need for ongoing immunosuppressive therapy
  • Recent history (<2 weeks) of CVA
  • Aspirin allergy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00292500

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Klinik für Herzchirurgie
Leipzig, Germany, D-04289
Sponsors and Collaborators
Cardica, Inc
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Principal Investigator: Jan Gummert, MD Herzzentrum Leipzig Gmbh
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Responsible Party: Cardica, Inc Identifier: NCT00292500    
Other Study ID Numbers: IP2004-06
First Posted: February 16, 2006    Key Record Dates
Last Update Posted: August 21, 2013
Last Verified: August 2013
Keywords provided by Cardica, Inc:
CABG, anastomotic device; myocardial revascularization
Additional relevant MeSH terms:
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Coronary Artery Disease
Coronary Disease
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Arterial Occlusive Diseases
Vascular Diseases