Clinical Trial: A Study to Determine Pharmacokinetic Changes of Ceftriaxone in Patients With Liver Cirrhosis
Study Status: COMPLETED
Recruit Status: COMPLETED
Condition: Antibiotic Toxicity
Study Type: OBSERVATIONAL
Official Title: An Observational Explorative Study to Determine Pharmacokinetic Changes of Ceftriaxone in Blood and Ascites in Patients Admitted With Decompensated Liver Cirrhosis With or Without Renal Impairment.
Brief Summary:
The investigators designed an observational multicenter explorative in vivo study to investigate the changes in ceftriaxone pharmacokinetics in blood and ascites.The investigators will include a total of 20 patients with liver cirrhosis admitted to the ward of participating hospitals.Patients are eligible when receiving ceftriaxone and concomitantly receive paracentesis.The investigators will collect all available waste blood samples of each participant, starting from study entry up until 48 hours after the last…
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