Coronary Artery Disease Clinical Trial
Official title:
Comparison of "One-stop" Hybrid Coronary Revascularization Versus Off-pump Coronary Artery Bypass for the Treatment of Multi-vessel Coronary Artery Disease
The "one-stop" hybrid coronary revascularization combines minimally invasive direct coronary artery bypass (MIDCAB) and PCI to be performed in the hybrid operating suite, an enhanced operating room equipped with radiographic capability. This study is to compare 1-year clinical outcomes of "one-stop" hybrid coronary revascularization with off-pump coronary artery bypass (OPCAB) in selected patients with multivessel coronary artery disease.
- With the development of specialized devices and experience, off-pump coronary artery
bypass (OPCAB) has been a well-established less invasive technique for coronary
revascularization. Compared with conventional on-pump coronary artery bypass grafting
(CABG), OPCAB avoids the use of cardiopulmonary bypass and cardioplegic arrest, and is
associated with decreased morbidity, shorter length of stay in ICU and hospital, and less
perioperative complications, especially in elderly patients with severe comorbidities.
"One-stop" (also named simultaneous) hybrid coronary revascularization is also a novel, safe
and feasible minimally invasive approach in selected patients with multivessel coronary
artery disease (CAD). It allows surgical and interventional procedures to be performed
consecutively in the "one-stop" hybrid operating suite, an enhanced operating room equipped
with radiographic capability, wherein the left intramammary artery (LIMA) is placed on the
left anterior descending artery (LAD) by minimally invasive procedure, immediately followed
by percutaneous coronary intervention/stenting on the non-LAD lesions. However, few studies
are now available on the outcomes of coronary revascularization between the new hybrid
strategy with conventional OPCAB. This study is a single center randomized clinical trial to
compare 1-year clinical outcomes of "one-stop" hybrid coronary revascularization with OPCAB
in selected patients with multivessel CAD with suitable coronary anatomy.
Sample size:
- We examined the results of SYNTAX trial and of our institution published previously. The
1-year MACCE rate (the primary endpoint) is estimated as being 13% for OPCAB. The sample
calculated for this trial is 400 patients.
Design/Methodology:
- Trial design: A single center randomized clinical trial comparing "one-stop" hybrid
procedure versus conventional OPCAB in 400 patients with suitable anatomy who need
revascularization.
Intervention: Patients will be randomized to undergo either "one-stop" hybrid procedure or
conventional OPCAB.
- Randomization: Patients will be evaluated by both a cardiac surgeon and an interventional
cardiologist. After obtaining informed written consent, patients will be randomized to
receive "one-stop" hybrid procedure or conventional OPCAB. An expertise-based randomization
will be used.
The data adjudicators will be blinded to the study. Due to the nature of this study, the
operating surgeons, cardiologists, anesthetists, other operative room staff, and ICU staff
will not be blind in this study.
Study intervention:
- Candidates will be randomized to receive "one-stop" hybrid procedure or conventional
OPCAB.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT06030596 -
SPECT Myocardial Blood Flow Quantification for Diagnosis of Ischemic Heart Disease Determined by Fraction Flow Reserve
|
||
| Completed |
NCT04080700 -
Korean Prospective Registry for Evaluating the Safety and Efficacy of Distal Radial Approach (KODRA)
|
||
| Recruiting |
NCT03810599 -
Patient-reported Outcomes in the Bergen Early Cardiac Rehabilitation Study
|
N/A | |
| Recruiting |
NCT06002932 -
Comparison of PROVISIONal 1-stent Strategy With DEB Versus Planned 2-stent Strategy in Coronary Bifurcation Lesions.
|
N/A | |
| Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
| Recruiting |
NCT04242134 -
Drug-coating Balloon Angioplasties for True Coronary Bifurcation Lesions
|
N/A | |
| Recruiting |
NCT05308719 -
Nasal Oxygen Therapy After Cardiac Surgery
|
N/A | |
| Completed |
NCT04556994 -
Phase 1 Cardiac Rehabilitation With and Without Lower Limb Paddling Effects in Post CABG Patients.
|
N/A | |
| Recruiting |
NCT05846893 -
Drug-Coated Balloon vs. Drug-Eluting Stent for Clinical Outcomes in Patients With Large Coronary Artery Disease
|
N/A | |
| Recruiting |
NCT06027788 -
CTSN Embolic Protection Trial
|
N/A | |
| Recruiting |
NCT05023629 -
STunning After Balloon Occlusion
|
N/A | |
| Completed |
NCT04941560 -
Assessing the Association Between Multi-dimension Facial Characteristics and Coronary Artery Diseases
|
||
| Completed |
NCT04006288 -
Switching From DAPT to Dual Pathway Inhibition With Low-dose Rivaroxaban in Adjunct to Aspirin in Patients With Coronary Artery Disease
|
Phase 4 | |
| Completed |
NCT01860274 -
Meshed Vein Graft Patency Trial - VEST
|
N/A | |
| Recruiting |
NCT06174090 -
The Effect of Video Education on Pain, Anxiety and Knowledge Levels of Coronary Bypass Graft Surgery Patients
|
N/A | |
| Terminated |
NCT03959072 -
Cardiac Cath Lab Staff Radiation Exposure
|
||
| Completed |
NCT03968809 -
Role of Cardioflux in Predicting Coronary Artery Disease (CAD) Outcomes
|
||
| Recruiting |
NCT04566497 -
Assessment of Adverse Outcome in Asymptomatic Patients With Prior Coronary Revascularization Who Have a Systematic Stress Testing Strategy Or a Non-testing Strategy During Long-term Follow-up.
|
N/A | |
| Recruiting |
NCT05065073 -
Iso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography
|
Phase 4 | |
| Completed |
NCT05096442 -
Compare the Safety and Efficacy of Genoss® DCB and SeQuent® Please NEO in Korean Patients With Coronary De Novo Lesions
|
N/A |