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Clinical Trials/DRKS00030889
DRKS00030889RecruitingUnknown

Influence of extracorporeal circulation on perioperative cefuroxime concentrations in bypass surgery patients.Exploratory, prospective, open-label, monocentric study to investigate the influence of operative extracorporeal circulation on perioperative cefuroxime concentrations using microdialysis technique in bypass surgery patients

niversitätsklinikum Augsburg0 sites30 target enrollmentStarted: June 27, 2023Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Recruiting
Sponsor
Enrollment
30

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomized controlled study
Masking
Open (masking not used)

Eligibility Criteria

Ages
18 Years to one (—)
Sex
All

Inclusion Criteria

  • Patients undergoing elective bypass surgery who require perioperative antibiotic prophylaxis
  • - Written declaration of consent by the patient

Exclusion Criteria

  • - Patients who have received therapy with cefuroxime in the 72 hours prior to surgery.
  • - Known allergic reaction, hypersensitivity or contraindication to cefuroxime or other ß-lactam antibiotics (e.g. penicillins, cephalosporins).
  • - Severe renal insufficiency < 20 ml/min/1.73 m2
  • - Non-guideline discontinuation of blood thinning medications
  • Medications if urgency does not allow the surgery to be postponed for the appropriate number of days.
  • - Active participation in other interventional studies according to AMG or MPDG
  • - Women during pregnancy or breastfeeding

Investigators

Sponsor
niversitätsklinikum Augsburg

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