Coronary Artery Disease Clinical Trial
Official title:
A Multicenter Randomized Trial to Compare the Graft Patency Between No-Touch Vein Harvesting Technique and Conventional Approach in Coronary Artery Bypass Graft Surgery: the PATENCY Study
Verified date | October 2019 |
Source | China National Center for Cardiovascular Diseases |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates the short-term patency of vein graft harvested by the No-Touch technique compared to that by the conventional approach in patients undergoing isolated on-pump/off-pump coronary artery bypass graft (CABG) surgery. a total of at least 2000 patients undergoing isolated on-pump/off-pump CABG will be consecutively recruited from 7 hospitals across China and randomly assigned to receive No-Touch saphenous vein harvesting or conventional approach. All participants will be invited for clinical follow-up and 64-slice multislice computed tomography angiography (MSCTA) analysis at 3 months post-operatively.
Status | Active, not recruiting |
Enrollment | 2655 |
Est. completion date | December 30, 2020 |
Est. primary completion date | September 30, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients receiving first time isolated on-pump/off-pump CABG - Patients with at least one available saphenous vein graft Exclusion Criteria: - Need for a concomitant cardiac or vascular surgeries (i.e. valve repair or replacement, Maze surgery) - Redo-CABG - Emergent CABG - Using vascular stapler for anastomosis - Endarterectomy of coronary artery during surgery - Left ventricular repair due to ventricular aneurysm - Combined with malignant tumor or other severe systemic conditions - Severe renal insufficiency (i.e. creatinine >200 µmol/L) - Contraindications for dual antiplatelet therapy, such as active gastroduodenal ulcer - Participants of another ongoing clinical trials |
Country | Name | City | State |
---|---|---|---|
China | Fuwai Hospital Chinese Academay of Medical Science and National Center for Cardiovascular Diseases | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
China National Center for Cardiovascular Diseases |
China,
Wang X, Tian M, Zheng Z, Gao H, Wang Y, Wang L, Hu S. Rationale and design of a multicenter randomized trial to compare the graft patency between no-touch vein harvesting technique and conventional approach in coronary artery bypass graft surgery. Am Heart J. 2019 Apr;210:75-80. doi: 10.1016/j.ahj.2018.11.011. Epub 2018 Dec 6. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Prevalence of graft occlusion | All participants will be invited to return to their operating hospitals for 64-slice multi-slice computed tomography angiography to determine patencies of the graft vessels. | 3 month after procedure | |
Secondary | Prevalence of graft occlusion | All participants will be invited to return to their operating hospitals for 64-slice multi-slice computed tomography angiography to determine patencies of the graft vessels. | 1 year after procedure | |
Secondary | Overall major adverse cardiac or cerebrovascular events (MACCE) rate | MACCE includes death, myocardial infarction, stroke and/or repeat revascularization | 3 month and 1 year after procedure | |
Secondary | Cardiac death | death from any heart disease | 3 month and 1 year after procedure | |
Secondary | Documented non-lethal myocardial infarction | Myocardial infarction is defined according to the most recent guideline | 3 month and 1 year after procedure | |
Secondary | Stroke | an acute symptomatic episode of focal or global neurological dysfunction caused by brain, spinal, or retinal vascular injury as a result of hemorrhage or infarction | 3 month and 1 year after procedure | |
Secondary | Target lesion revascularization | CABG or percutaneous coronary intervention | 3 month and 1 year after procedure | |
Secondary | Recurrence of Angina | recurrence of unstable angina | 3 month and 1 year after procedure |
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