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CompletedNCT03034174

Pharmacokinetics of High-dose Tigecycline in Critically Ill Patients

Pharmacokinetics of High-dose Tigecycline in Critically Ill Patients: an Observational, Prospective Study

Status
Completed
Phase
Study type
Observational
Enrollment
37 (actual)
Sponsor
Medical University of Lublin · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to describe the pharmacokinetics of tigecycline in critically ill patients receiving continuous venovenous haemodialysis (CVVHD) and to evaluate the frequency of pharmacokinetic/pharmacodynamic target attainment with high dosing strategy (200 mg loading dose and 100 mg/12h).

Detailed description

This is a prospective observational study performed on critically ill patients. Inclusion criteria are: severe sepsis on admission requiring broad-spectrum antibiotics. Both medical and surgical patients will be included. Any type of infections will be included (pulmonary, abdominal, urinary tract, etc.) Antibiotics regimen includes: tigecycline (200 mg every 12 hours intravenously), meropenem (2 grams every 8 hours intravenously). Blood samples (3 mL) will be collected 2, 4, 8 and 12 hours after each dose of tigecycline for 3 consecutive days. The standard arterial canula will be used to obtain samples. In each case CVVHD will be started and continued for at least 3 days' period. 30 minutes after a collection each sample will be centrifuged for 10 minutes at 3,000 rpms. Subsequently, supernatant will be collected and frozen. Serum tigecycline concentration will be measured with high performance liquid chromatography. Each patient's hemodynamics parameters will be recorded with the use of transpulmonary thermodilution technique (PICCO). Other therapies i.e.: ventilatory support, sedation, an antifungal agent will be given as required.

Conditions

Timeline

Start date
2017-01-15
Primary completion
2017-12-15
Completion
2018-10-10
First posted
2017-01-27
Last updated
2023-11-24

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT03034174. Inclusion in this directory is not an endorsement.

Pharmacokinetics of High-dose Tigecycline in Critically Ill Patients (NCT03034174) · Clinical Trials Directory