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Cell Salvage and Retrograde Autologous Priming

U

University Hospital Schleswig-Holstein (UKSH)

Status

Completed

Conditions

Hemodynamic Instability
Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT04792814
IN-MAT_RAP_01

Details and patient eligibility

About

In recent years Patient Blood Management (PBM) has developed into a multifactorial and interdisciplinary concept that focuses on individualized and optimized hemotherapy. Of course, this also applies to the cardiac surgery area (1). In this context, the quality of the intraoperative PBM can be represented by patients scheduled for isolated coronary artery bypass grafting (CABG) and isolated aortic valve replacement (AVR). In a prospective, observational "before-and-after" protocol, the investigators analysed the impact of the combined use of retrograde autologous priming (RAP) and cell salvage on intraoperative usage of red blood cell concentrates (RBC) (2).

Full description

200 patients (CABG or AVR) will be monitored using local standard of care in these patients without cell salvage and RAP (control group, CG), followed by 200 patients with cell salvage and RAP (study group, SG). Both groups are defined by elective surgery and hemodynamically stable patients prior to the onset of the cardiopulmonary bypass (CPB). Based on our own data and current data from the literature, the investigators assume that the use of MAT in combination with RAP leads to at least an intraoperative reduction of the erythrocyte consumption of 15%. Consequently, the investigators calculated a case number of approximately 200 patients per group.

The study is set up with a control group under previous standard therapy. The data is recorded and analyzed descriptively. Qualitative comparisons will be made in the discussion of previously published data.

Enrollment

200 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • scheduled for cardiac surgery
  • informed written consent

Exclusion criteria

  • rejection by the patient
  • switching to another procedure

Trial design

200 participants in 2 patient groups

MAT-RAP group
Description:
MAT and RAP
historical group
Description:
standard procedure

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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