NCT05740397 Trial to Compare Different Strategies of Mean Arterial Pressure Management During Cardiopulmonary By-pass
| NCT ID | NCT05740397 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Azienda Ospedaliera Universitaria Integrata Verona |
| Condition | Heart; Surgery, Heart, Functional Disturbance as Result |
| Study Type | INTERVENTIONAL |
| Enrollment | 900 participants |
| Start Date | 2021-05-03 |
| Primary Completion | 2023-12-31 |
Eligibility & Interventions
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 900 participants in total. It began in 2021-05-03 with a primary completion date of 2023-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
* Background: One of the main goals of the Cardiopulmonary By-Pass (CPB) is targeting an adequate Mean Arterial Pressure (MAP), in order to maintain appropriate perfusion pressures in all end-organs during heart surgery. As inheritance of early studies, a value of 50-60 mmHg has been historically accepted as the "gold standard" MAP. However, in the last decades, the CPB management has remarkably changed, thanks to the evolution of technology and the availability of new biomaterials. Therefore, as already highlighted by the latest European Guidelines, the current management of CPB can no longer refer to those pioneering studies. To date, only few single-centre studies have compared different strategies of MAP management during CPB, but with contradictory findings and without achieving a real consensus. Therefore, what should be the ideal strategy of MAP management during CPB is still on debate. This trial will be the first multicentre, randomized, controlled study to compare three different strategies of MAP management during the CPB. * Methods: We described herein the methodology of a multicenter, randomized, controlled trial comparing three different approaches to MAP targeting during CPB in patients undergoing elective cardiac surgery: the historically accepted "standard MAP" (50-60 mmHg), the "high MAP" (70-80 mmHg) and the "patient-tailored MAP" (comparable to the patient's preoperative MAP). It is the aim of the study to find the most suitable management in order to obtain the most adequate perfusion of end-organs during cardiac surgery. For this purpose, the primary endpoint will be the peak of serum lactate (Lmax) released during CPB, as index of tissue hypoxia. The secondary outcomes will include all the intraoperative parameters of tissues oxygenation and major post-operative complications related to organ malperfusion. * Discussion: This trial will assess the best strategy to target the MAP during CPB to further improve the outcomes of cardiac surgery.
Eligibility Criteria
Inclusion Criteria: * Elective surgery * Index of surgical risk Euroscore II \< 9% * The following procedures will be considered: Isolated or combined with aortic or mitral valve surgery coronary artery bypass graft surgery for acute or chronic coronary artery disease isolated aortic valve replacement for aortic stenosis and/or aortic regurgitation ; isolated mitral valve repair or replacement for mitral stenosis and/or mitral regurgitation; isolated ascending aorta surgery with or without aortic valve replacement * Surgical approach through complete and/or mini-sternotomy * Preserved or mildly reduced left ventricular ejection fraction (LVEF ≥ 40%) at preoperative echocardiography * Patients with an estimated Glomerular filtration rate (eGFR) ≥ 40 ml/min/mq calculated using the Modification of Diet in Renal Disease formula (MDRD) * Signed informed consent Exclusion Criteria: * Age \< 18 years and \>80 years * Reoperation * Emergent, urgent and salvage procedures * Euroscore II \> 9% * Right toracothomy procedures * Any surgical procedure not listed above (i.e. tricuspid valve surgery, aortic root surgery, congenital heart diseases, surgery necessitating hypotermic circulation arrest, surgical ablation of atrial fibrillation etc.) * More than mild left ventricular dysfunction at preoperative echocardiogram (LVEF \< 40%) * Patients with critical preoperative state: any ventricular fibrillation or ventricular tachycardia, preoperative cardiac massage, preoperative ventilation before anaesthetic room, preoperative inotropes or mechanical circulatory support planned before cardiac intervention (i.e. during coronary angiography) and other conditions according to Euroscore II definition. * Patients with an estimated eGFR \< 40 ml/min/mq calculated using the MDRD or patients on dialysis. * Patients with chronic obstructive pulmonary disease \> 3 stage according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2019 classification. * Patients with severe preoperative epatic failure (CHILD-PUGH ≥ B) * Patient with severe symptomatic carotid atheromasia
Contact & Investigator
Frequently Asked Questions
Who can join the NCT05740397 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Heart; Surgery, Heart, Functional Disturbance as Result. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05740397 currently recruiting?
Yes, NCT05740397 is actively recruiting participants. Contact the research team at alessandrafrancica@yahoo.it for enrollment information.
Where is the NCT05740397 trial being conducted?
This trial is being conducted at Verona, Italy.
Who is sponsoring the NCT05740397 clinical trial?
NCT05740397 is sponsored by Azienda Ospedaliera Universitaria Integrata Verona. The trial plans to enroll 900 participants.