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

NCT00292500 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 170

Last updated 2013-08-21

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Automated distal anastomotic device

CABG

Sponsors & Collaborators

  • Cardica, Inc

    lead INDUSTRY

Principal Investigators

  • Jan Gummert, MD · Herzzentrum Leipzig Gmbh

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
50 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2008-10-31
Completion
2009-12-31

Countries

  • Germany

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00292500 on ClinicalTrials.gov