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Combined Use of a Novel Cardioplegic Formula With MPS® Versus Cardioplexol ® in Urgent Isolated CABG Using MiECC in Patients With Recent Acute Myocardial Infarction

Combined Use of a Novel Cardioplegic Formula With MPS® Versus Cardioplexol ® in Urgent Isolated CABG Using MiECC in Patients With Recent Acute Myocardial Infarction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04309994
Enrollment
307
Registered
2020-03-17
Start date
2010-02-01
Completion date
2020-01-31
Last updated
2020-03-17

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

Conditions

Cardioplegia Solution Adverse Reaction, Coronary Artery Bypass Grafting (CABG), Heart Attack

Keywords

heart attack, cardioplegia solution, Minimal extracorporeal circulation system (MiECC), Myocardial protection system (MPS), Coronary artery bypass grafting (CABG)

Brief summary

The goal of this study is to compare the two cardioplegia solutions (blood cardioplegia by means of MPS ® vs. Cardioplexol ®) regarding perioperative outcome and with special attention to cardiac markers in patients with a recent heart attack.

Interventions

OTHERMyocardial protection system (MPS)

cardioplegia solution, A separate pumpsystem by which Blood cardioplegia with individually composable additives as cardioplegia solution can be used

OTHERCardioplexol

cardioplegia solution

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Patients who underwent a CABG using MPS® or Cardioplexol ® * Heart attack less than 7 days before surgery

Exclusion criteria

* use of other cardioplegia solution than Cardioplexol ® or MPS® * other inventions than CABG * explicit will of the patient that his data may not be used * denied general consent

Design outcomes

Primary

MeasureTime frameDescription
myocardial damagepatients with that received a coronary artery bypass grafting and that were treated (for approximately 15 days) at the University Hospital between February 2010 and January 2020 (data taken perioperative during hospital stay for CABG)Analyse cardiac biomarkers as indicators for myocardial damage: high sensitive troponin (Ths-TrT, ng/mL), creatine kinase (CK, in ng/mL) and creatine kinase-MB isoenzyme (CK-MB, in ng/mL)

Secondary

MeasureTime frameDescription
30 days Mortality30 days after CABGdeath after coronary artery bypass grafting
length of stay in the intensive care unitperioperative during hospital stay for CABG (for approximately 15 days)duration of stay at intensive care unit
Number of participants with bleedingsperioperative during hospital stay for CABG (for approximately 15 days)bleeding complication after coronary artery bypass grafting
Number of participants with postoperative arrhythmiaperioperative during hospital stay for CABG (for approximately 15 days)rhythm disturbance after coronary artery bypass grafting

Countries

Switzerland

Outcome results

None listed

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