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Long Term Follow-up Hybrid Revascularization

Completed
Conditions
Coronary Artery Disease
Interventions
Procedure: Robotic Hybrid coronary artery revascularization
Registration Number
NCT01955330
Lead Sponsor
Lawson Health Research Institute
Brief Summary

OBJECTIVES:

The objectives of the year study are two-fold:

1. To determine the 5-7 year patency rate (rate of open bypass grafts) of the LITA graft and stent of patients who have already had robotically-assisted Hybrid CABG surgery using CTA and MPS-MIBI.

2. To determine patient quality of life at 5-7 years after robotically-assisted Hybrid CABG surgery

Detailed Description

New techniques such as robotically-assisted Hybrid CABG surgery need proper evaluation to ensure potential benefits gained are not harmful to that which we know to be of significant benefit to the patients, that being the left internal thoracic artery (LITA) graft (one of the main coronary arteries supplying your heart with blood). We are therefore proposing a 5-7 year CT-Angiography (CTA) and Myocardial Perfusion Scintigraphy (MPS-MIBI) to assess the patency rate of the LITA graft and the stented graft in patients that have already undergone robotically assisted Hybrid CABG.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Patients that have previously had Hybrid robotic coronary artery revascularization performed approximately 5-7 years ago at the London Health Sciences Centre, University Hospital by Dr. Kiaii.
Exclusion Criteria
  • Patients not described above

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Hybrid robotic cabg patientsRobotic Hybrid coronary artery revascularizationPostoperative (5-7 years)Hybrid CABG robotically assisted surgical revascularization patients
Primary Outcome Measures
NameTimeMethod
Graft patency5-7 years post Hybrid surgery

To assess the graft patency of the LITA to LAD performed by the robot and the patency of the Stent.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

London Health Sciences Centre, University & Victoria Hospitals

🇨🇦

London, Ontario, Canada

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