Study of Tigecycline Pharmacokinetics in Patients Undergoing Continuous Renal Replacement Therapy(CRRT)
Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
The aim of this study is to determine the Pharmacokinetics/Pharmacodynamics(PK/PD) of
tigecycline in critical ill patients undergoing continuous renal replacement therapy（CRRT）and
examine whether the dosage needs adjustment.
The study will observe two groups of patients respectively and compare the difference between
them. Patients who need to receive CRRT when treat with high-dose tigecycline will be
collected in Group CRRT. Patients who treat with high-dose tigecycline only will be collected
in Group non-CRRT.