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Clinical Trial ● Currently Recruiting Non-phase study NCT05487612

MiECC Versus Conventional Cardiopulmonary Bypass in Cardiac Surgery (MiECS)

MiECC Versus Conventional Cardiopulmonary Bypass in Cardiac Surgery (MiECS) — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT05487612.

📅 30 Mar 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT05487612
Sponsor
Aristotle University Of Thessaloniki
Start
2022-05-26
ClinicaliQ Trial Snapshot
  • MiECC Versus Conventional Cardiopulmonary Bypass in Cardiac Surgery (MiECS) — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT05487612.
  • MiECS is one of the largest multicentre randomised controlled trials on extracorporeal circulation conducted under the auspices of Minimal Invasive Extracorporeal Technologies International Society (MiECTiS). It is designed to ultimately address the emerging effectiveness of MiECC systems in the light of modern….
  • Sponsor: Aristotle University Of Thessaloniki.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

Use This Page For
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  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

MiECS is one of the largest multicentre randomised controlled trials on extracorporeal circulation conducted under the auspices of Minimal Invasive Extracorporeal Technologies International Society (MiECTiS). It is designed to ultimately address the emerging effectiveness of MiECC systems in the light of modern perfusion practice worldwide. The primary hypothesis is that MiECC, as compared to conventional CPB (cCPB), reduces the proportion of patients experiencing serious perfusion-related postoperative morbidity after cardiac surgery. The study will be led by the Clinical Research Unit of the Special Unit for Biomedical Research and Education (SUBRE),…

Eligibility Snapshot
  • : * All patients undergoing any elective or urgent coronary artery bypass grafting (CABG), aortic valve replacement (AVR) or CABG+AVR surgery using extracorporeal circulation without circulatory arrest.

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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