Coronary Artery Disease (CAD) Clinical Trial
Official title:
Hybrid Revascularisation by Combined CABG and PCI in Multivessel Coronary Disease. An Observational Study.
The present study is designed as a prospective, single centre, open label, observational
trial.
The study will collect information about the medical care patients receive during their
planned procedure(s). No new testing or procedures will be done.
Patients elected for hybrid revascularization will be asked their written consent to the use
of their personal data.
Left internal mammary artery to the Left Anterior Descending Coronary Artery
(LIMA-LAD)surgical revascularization will be performed first, followed by percutaneous
revascularization of the other vessels in the frame of the same hospitalization.
After discharge patients will attend clinic visits at 30 days and 12 months, as per usual
clinical practice, and will be contacted by phone at 6 months after procedure. Angiographic
follow-up will be performed in symptomatic patients, as clinically indicated.
Hybrid coronary revascularization integrates the positive features of both Percutaneous
Coronary Intervention (PCI) and Coronary Artery Bypass Graft (CABG), combining the
durability of Left Anterior Descending Coronary Artery (LIMA) coronary bypass with the
minimal invasiveness and lower risk of percutaneous intervention. Thereby it might represent
a better option in a sizeable proportion of patients.
Candidate patients in whom hybrid revascularization would be advantageous are several
subgroups of Coronary Artery Disease (CAD) patients that are increasing in numbers: the
elderly patients with a high risk of mortality and/or morbidity for CABG, patients with
significant disabilities and patients in whom treatment durability is important but a
significantly invasive approach is not an option.
There are several potential advantages of the hybrid procedure over conventional CABG in
selected patients. These advantages include the avoidance of cardiopulmonary bypass-related
morbidity, no aortic manipulation with the LIMA-LAD with the beating heart procedure, less
blood loss and decreased transfusions, a shorter recovery time than after conventional CABG
and patient's preference for "minimally invasive" surgery.
The investigators hypothesize that in selected patients with diffuse coronary disease, a
"hybrid" approach employing a staged revascularisation procedure may allow to lower the
surgical risk, increase the completeness and effectiveness of revascularisation and,
hopefully, to improve immediate and long term outcome.
To test this hypothesis, a well designed, properly sized, prospective, randomized study is
needed. Available data, however, do not provide sufficient information to speculate on a
clinically meaningful, yet achievable, effectiveness.
Aim of this observational study is therefore to collect more information on the target
population, the clinical outcomes and optimal management in order to inform the design of a
comparative effectiveness trial.
;
Observational Model: Case-Only, Time Perspective: Prospective
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05292079 -
CAPTURER PMCF Study ( rEPIC04D )
|
||
Recruiting |
NCT05292014 -
ANGIOLITE PMCF Study ( rEPIC04F )
|
||
Recruiting |
NCT05292092 -
Essential Pro PMCF Study ( rEPIC04E )
|
||
Recruiting |
NCT05292118 -
Navitian PMCF Study ( rEPIC04C )
|
||
Completed |
NCT05292105 -
NC Xperience PMCF Study( rEPIC04B)
|
||
Completed |
NCT01435031 -
EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Eluting Coronary Stent Coronary Stents, Performance, and Technique in Chronic Total Occlusions
|
N/A | |
Completed |
NCT00783302 -
Study in Subjects Suspected of Having CAD Undergoing VISIPAQUE-enhanced CCTA as Part of Their Routine Medical Care
|
N/A | |
Completed |
NCT00543400 -
Evaluation of M118 in Percutaneous Coronary Intervention (EMINENCE)
|
Phase 2 | |
Completed |
NCT05516784 -
Impact of CYP2C19 Genotype-guided Clopidogrel and Ticagrelor Treatment on Platelet Function Test and Metabolomics Profile
|
Phase 4 | |
Completed |
NCT02873052 -
MyoVista Measurements in Patients With Atherosclerosis and CAD
|
||
Terminated |
NCT02984891 -
Optical Coherence Tomography (OCT) Intravascular Ultrasound (IVUS) Dual Imaging
|
||
Completed |
NCT05292144 -
Xperience Pro PMCF Study
|
||
Completed |
NCT02554292 -
Post Market Surveillance of SeQuent Please Neo With Scoring Balloon
|
||
Active, not recruiting |
NCT06052319 -
A Study to Assess the Engagement and Usefulness of Care4Today Digital Platform for Disease Management in Coronary Artery Disease (CAD) and/or Peripheral Artery Disease (PAD) Population
|
||
Completed |
NCT00265525 -
Evaluation of a Web-based Intervention to Promote Physical Activity in Patients With Heart Disease.
|
Phase 3 | |
Completed |
NCT03570697 -
Imaging of Coronary Plaques in Participants Treated With Evolocumab
|
Phase 3 | |
Terminated |
NCT05508893 -
Screening for Coronary Artery Disease USing Primary Evaluation With Coronary CTA in Aviation Medicine (SUSPECT)
|
N/A | |
Completed |
NCT02341664 -
Patient and Provider Assessment of Lipid Management Registry
|
||
Completed |
NCT02098772 -
Phase III Study Comparing Two Methods of Cardioplegia in Aortic Valve Surgery Custodiol-N Versus Custodiol
|
Phase 3 | |
Recruiting |
NCT05617599 -
SUPRAFLEX CRUZ PMCF Study ( rEpic05 )
|