antibiotic concentrations (cefuroxime) antifibriniolytics (tranexamic acid) D68.9
Conditions
Interventions
Group 1: Single arm, open, observational, non-randomized clinical trial to evaluate the perioperative pharmacokinetcis of cefuroxime and tranexamic acid with and without the use of cardiopulomonary by
Sponsors
Deutsches Herzzentrum München
Eligibility
Sex/Gender
All
Age
No minimum to 12 Months
Inclusion criteria
Inclusion criteria: Pediatric cardiac patients less than one year of age undergoing cardiac surgery with and without cardiopulmonary bypass.
Exclusion criteria
Exclusion criteria: Participation in any interventional study. Pretreatment with antibiotics and tranexamic acid.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Chromatographic determination of serum concentrations of cefuroxime and tranexamic acid with and without the use of cardiopulmonary bypass. | — |
Secondary
| Measure | Time frame |
|---|---|
| Determination of elimination half life, Clearance, AUC, maximaler Serumkonzentration Cmax and mean residence time (MRT) for both substances. | — |
Countries
Germany
Contacts
Public ContactRalph Gertler
Klinikum Links der Weser
Outcome results
None listed