Skip to content

Impact of Total Coronary Revascularization Via Left Anterior Thoracotomy (TCRAT) vs. Robotic-Assisted Harvesting of LIMA (ITcrats)

Impact of Total Coronary Revascularization Via Left Anterior Thoracotomy (TCRAT) vs. Robotic-Assisted Harvesting of Left Internal Thoracic Artery on Hospital Stay (ITcrats)

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06988735
Acronym
ITcrats
Enrollment
182
Registered
2025-05-25
Start date
2025-07-31
Completion date
2027-08-31
Last updated
2025-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Elective Surgery, Minimally Invasive Coronary Revascularization Surgery

Keywords

minimally invasive coronary revascularization surgery, robotic-assisted coronary artery bypass graft (RA-CABG), major adverse cardiovascular events (MACCE), major adverse cerebrovascular events, cardiopulmonary bypass (CPB), hospital stays, costs and charges

Brief summary

The two types of total coronary revascularization via left anterior thoracotomy (TCRAT) might have their potential benefits and disadvantages. The proposed randomized clinical trial here will compare 'RA-TCRAT' with 'Nonrobotic TCRAT' procedures concerning effects on hospital stays, overall healthcare costs, safety, and feasibility. If the two TCRAT procedures are comparably effective and safe, the 'Nonrobotic TCRAT' procedure is probably preferred as it seems easier to use. However, if the 'Nonrobotic TCRAT' procedure is less effective and less safe than the robotic TCRAT,' that procedure should be preferred.

Detailed description

Rationale A recent study involving 1,195 patients from the Society of Thoracic Surgeons Registry undergoing robotic-assisted-minimally-invasive direct coronary artery bypass (RA-MIDCAB) by 114 surgeons between 2014 and 2019 showed that surgeons can quickly reduce complication rates by building up the learning curve. It is yet unclear if robotic-assisted harvesting of the left internal thoracic artery (RA-LITA) would offer a benefit over total coronary revascularization via left anterior thoracotomy (TCRAT) in terms of the postoperative hospital stay and cost of healthcare. That raises the need to examine the impact of RA-LITA compared with TCRAT on these crucial clinical outcomes. Objective The primary objective of this prospective randomized clinical trial (RCT) is, compared with TCRAT, to examine the impact of robotic-assisted coronary artery bypass graft (RA-CABG) on the length of hospital stay in diverse patients scheduled for elective surgical coronary revascularization. Secondary objectives include identifying the overall costs and charges of healthcare, operating room and intensive care unit (ICU) stays, postoperative bleeding, need for re-explorative surgery or transfusion, postoperative major adverse cardiovascular and cerebrovascular events (MACCE)\], acute kidney injury (AKI), and surgical related complications and 30-days and 3-months need for hospital re-admission and survival after adult cardiac surgical coronary revascularization using cardiopulmonary bypass (CPB). Hypothesis It is hypothesized that RA-total coronary revascularization via left anterior thoracotomy (TCRAT) might have shorter hospital stays than the nonrobotic assisted TCRAT in adult patients undergoing elective coronary revascularization surgery. Nature and extent of the burden and risks associated with participation, benefit, and group relatedness There is no expected patient burden or risk other than the estimated risks for the coronary revascularization surgery. Patient burden and risks are low, and the two surgical approaches (nonrobotic TCRAT and RA-CABG/TCRAT) are being used widely and interchangeably. The collection of patients' outcome data from hospital charts and (electronic) medical records systems causes no harm to the patients; patients will not experience any discomfort from any of the study interventions because they will be performed during general anesthesia. INTRODUCTION AND RATIONALE 3.1 TCRAT has a significant impact on outcomes. The main goals of minimally invasive cardiac surgery (MICS) are to avoid sternotomy, reduce postoperative blood product transfusion, shorten ventilation times, shorten intensive care and hospital stays, improve the quality of postoperative analgesia, and expedite physical recovery. TECRAT emerged as a promising MICS procedure. TCRAT has been shown to have a likely success rate of 95%, defined as complete revascularization in a cohort of 102 multivessel coronary artery disease (MV-CAD) patients with diverse age, body mass index (BMI), and left-ventricular ejection fraction (LVEF) in conjunction with low incidences of in-hospital mortality, CVA, AMI and need for revascularization in 2%. Muliarterial TCRAT increased the aortic cross-clamping and operating room times without further improving these outcomes or shortening hospital stays. 3.2 Robotic totally endoscopic CABG (TE-CABG) Robotic TE-CABG is technically more challenging than RA-CABG. Kofer et al. compared the 12 years of single-center experience performing conventional CABG or TE-CABG in a propensity score-matched retrospective study. They identified similar age groups, log European System for Cardiac Operative Risk Evaluation (EuroSCORE), perioperative mortality, AMI, and stroke rate, and long-term survival and freedom from major adverse cardiac and cerebral events at 1, 5, and 10 years after surgery between the two groups. TE-CABG took 40% longer CPB and 67% cross-clamp times. That doubts the superiority of TE-CABG over the RA-MIDCAB or RA-TCRAT. 3.3. RA-MIDCAB MIDCAB is performed without the use of CPB with associated fewer complications such as perioperative CVA due to avoidance of aortic manipulation. CPB might be required in rare cases during MIDCAB procedures that necessitate peripheral cannulation to avoid a sternotomy, which could be challenging in patients with severe peripheral vascular disease and morbidly obese patients who would benefit the most from avoiding a sternotomy. A RA-MIDCAB procedure may be possible in such patients. Patrick et al. demonstrated a growing learning curve after the 10th RA-MIDCAB procedure in terms of reduced rates of approach conversion (odds ratio, 0.27; 95% CI, 0.09-0.84) and improved procedural success (odds ratio, 1.96; 95% CI, 1.00-3.84). A cohort of 605 RA-MIDCAB patients performed at a single center over 18 years showed a reduced conversion rate to sternotomy for any cause, from 16.0% of the first 200 cases to 6.9% of the last 405 patients. The mortality rate was 0.3%, the patency rate of the LITA-to-left anterior descending (LAD) coronary artery anastomosis was 97.4%, surgical re-exploration for bleeding in 1.8% of patients, and the transfusion rate was 9.2%. A previous study found that compared with those who underwent conventional CABG (n=235), patients who received RA-CABG (n=281) had fewer risk factors, lower in-hospital and long-term mortality but had comparable incidences of target lesion revascularization (TLR), target vessel revascularization (TVR), AMI, and stroke. Interestingly, neither the residual Synergy Between Percutaneous Coronary Intervention With Taxus and Cardiac Surgery (SYNTAX) score nor completeness of revascularization were related to the long-term mortality. 3.4. RA-CABG: An emerged approach to improve outcomes A retrospective study demonstrated that compared with MIDCAB, RA-CABG had comparable complete revascularization, one-year graft patency, surgical conversion, mortality rates, more extended operating room stays, and shorter ICU stays. To our knowledge, no RCT compares the impacts of TCRAT and RA-TCRAT CABG on successful revascularization, mortality, and postoperative CVA and AMI. 3.5. Feasibility The two types of TCRAT (nonrobotic or R.A.) have never been compared in terms of feasibility. 'RA-TCRAT' procedures are more complex to perform and might take longer durations to be accomplished, increasing the overall healthcare costs, which could be unacceptable for both the stakeholders. 'Non-RA-TCRAT' procedures are more straightforward to perform and are thus easier to learn, but most importantly, they take much less time.

Interventions

PROCEDURENonrobotic TCRAT

Nonrobotic TCRAT for CABG

PROCEDURERobotic TCRAT

Robotic TCRAT for CABG

Sponsors

Mohamed R El Tahan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Further minimization of bias will be achieved by involving two independent investigators. The researcher responsible for performing the surgery will perform the Randomization directly before the start of anesthesia. A second investigator, who will not be blinded for the randomization arm, will score the primary and secondary postoperative outcome measures.

Intervention model description

A single-center prospective randomized controlled clinical trial- and patient-blinded comparative trial in patients scheduled for surgical coronary revascularization. The RCT will be conducted according to Good Clinical Practice (GCP) Guidelines and comply with the principles of the Declaration of Helsinki. The RCT will be registered in a public registry, and the study protocol with its statistical analysis plan will be published before the enrollment of the first patient.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled for any type of elective minimally invasive coronary revascularization surgery. * Using CPB. * General anesthesia is provided in an endotracheally intubated patient

Exclusion criteria

* Planned for coronary revascularization surgery without CPB; * Planned for a combined coronary revascularization surgery and a valve or intra-cardiac surgery; * LVEF less than 35%; * Preoperative cardiogenic shock; * Pregnancy; * Scheduled for re-do or emergency surgery; * Consent for another interventional study during anesthesia; * No written informed consent; * Preoperative need for mechanical circulatory support; * Preoperative need for invasive ventilatory support;

Design outcomes

Primary

MeasureTime frameDescription
The length of hospital stayFor 120 days from surgeryThe primary outcome is the length of hospital stay, defined as the time from surgery until discharge or in-hospital death.

Secondary

MeasureTime frameDescription
The operating room stayFor 12 hours from entrance to the operating roomsThe operating room stays from entrance to transferring the patient to the ICU.
The postoperative ICU stayFor 120 days from surgeryThe postoperative ICU stay from surgery date and time.
The need for re-explorative surgery during the same admission.For 120 days from surgeryThe need for re-explorative surgery during the same admission.
Perioperative need for packed red blood cells (PRBCs) transfusionFor 72 hours from surgeryPerioperative need for transfusing packed red blood cells (PRBCs) 72 hours from surgery
Perioperative need for fresh frozen plasma (FFP) transfusionFor 72 hours from surgeryPerioperative need for transfusing fresh frozen plasma (FFP)
Perioperative need for platelets concentrate transfusionFor 72 hours from surgeryPerioperative need for transfusing platelets concentrate for 72 hours from surgery
Perioperative need for cryoprecipitates transfusionFor 72 hours from surgeryPerioperative need for transfusing cryoprecipitates transfusion for 72 hours from surgery
Perioperative need for recombinant factor VII administrationFor 72 hours from surgeryPerioperative need for administering recombinant factor VII for 72 hours from surgery
The cumulative postoperative chest tube outputsFor 48 hours after surgery.The cumulative postoperative chest tube outputs for 48 hours after surgery.
Any cause of in-hospital death during the same admissionFor 120 days from surgery until death or hospital dischargeAny cause of in-hospital death during the same admission
Overall costs and chargesFor 120 days from surgery until hospital discharge or deathThe overall healthcare costs and healthcare charges
In-hospital acute ischemic strokeFor 120 days from surgery until death or hospital dischargeThe incidence of in-hospital acute ischemic stroke until hospital discharge or in-hospital death.
In-hospital acute kidney injury (AKI)For 120 days from surgery until death or hospital dischargeThe incidence of in-hospital acute kidney injury (AKI) until hospital discharge or in-hospital death.
Need to intraoperative conversion to sternotomy.For 12 hours from the begining of surgeryNeed to intraoperative conversion from minimally-invasive thoracotomy to open sternotomy.
Graft's pulsatility index (P.I.).Intraoperatively after discontinuation of the CPBPost-CPB graft's pulsatility index (P.I.).
The need for postoperative coronary revascularizationFor 180 days from surgeryThe need for postoperative surgical or catheter angiographic coronary revascularization
In-hospital limb ischemiaFor 120 days from surgery until death or hospital dischargeThe incidence of limb ischemia until hospital discharge or in-hospital death.
The need for any-cause hospital re-admission within 30 days after surgery.For 30 days after surgery.The need for any-cause hospital re-admission within 30 days after surgery.
The need for any-cause hospital re-admission within 90 days after surgery.For 90 days after surgery.The need for any-cause hospital re-admission within 90 days after surgery.
All-cause mortality at 30 days after surgeryFor 30 days after surgeryAll-cause mortality at 30 days after surgery
All-cause mortality at 90 days after surgeryFor 90 days after surgeryAll-cause mortality at 90 days after surgery
In-hospital acute myocardial infarction (AMI)For 120 days from surgery until death or hospital dischargeThe incidence of in-hospital acute myocardial infarction (AMI) until hospital discharge or in-hospital death.

Countries

Saudi Arabia

Contacts

Primary ContactMoahmed R El Tahan, MD
mohamedrefaateltahan@yahoo.com0096569371849
Backup ContactYasser f ElGhoneimy, MD
yfarag@iau.edu.sa+966 59 777 7012

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026