Optimal Improvement of Vein Graft Patency Long Term by the Implementation Of Novel Endoscopic Harvesting Techniques
Completed
Conditions studied: Coronary Artery Disease
In brief
This is an observational study of lone Coronary Artery Bypass Grafting procedures with endoscopic vein graft harvesting using best harvesting practices.
Key facts
- Study ID
- NCT01697176
- Run by
- Cardiopulmonary Research Science and Technology Institute
- People needed
- 100
- Starts
- 2010-08-01
- Expected to finish
- 2014-08-01
- Last updated by the study team
- 2014-10-22
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age greater than 18 and able to provide consent
- Eligible for endoscopic vein harvesting
- Minimum of two non sequential vein grafts
- Willing to comply with requirements of protocol
You may not qualify if…
- Previous CABG
- Previous or concomitant valve surgery
- Any other concomitant cardiac procedure other than surgical ablation or incidental PFO repair
- Intolerance to Iodine or IV contrast that cannot be controlled with pre-medication
- Renal insufficiency with GFR measurement ≤ 40, unless dialysis dependent
- Abnormal platelet level defined as Plt Count >400,000
- Abnormal platelet function (hypercoagulable state) as evidenced by TEG testing
- Allergy to or presence of a condition that the investigator feels may prevent safe administration of ASA or Plavix post-operatively.
- Patient has a co-morbid condition that in the opinion of the investigator poses undue risk for successful endovascular harvesting of the vein
Where it is running
- CRSTI/Medical City Dallas — Dallas, Texas, United States
- The Heart Hospital Baylor Plano — Plano, Texas, United States
Full record on ClinicalTrials.gov
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