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Coupler Study.

Recruiting
Conditions
cabg, total arterial revascularization
Registration Number
NL-OMON20311
Lead Sponsor
Catharina Hospital Eindhoven.Sponsor: none
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

1. Able to give informed consent able to understand the intent and clinical meaning of the study as well as its implication;

2. Patients between 18 years and 70 years old;

Exclusion Criteria

1. Procedure is done as an emergency operation;

2. Unable to meet study requirements, i.e. mobility challenge;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Acute Patency: The presence of acute patency of the distal anastomoses as determined by flow measurements intraoperatively;<br /><br>2. Chronic Patency: The presence of patency of the end-to-end radial-lita anastomoses as determined by multislice CT - Scan at 3 months;<br /><br>3. Incidence of device related Adverse Events.
Secondary Outcome Measures
NameTimeMethod
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