Pharmacokinetics of Caspofungin

NCT03399032 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2023-11-24

No results posted yet for this study

Summary

The objective of this study is to describe the pharmacokinetics of standard doses of caspofungin in critically ill patients.

Conditions

Interventions

DRUG

Caspofungin

Each patient will receive: caspofungin i.v. once daily ( 70 mg on the first day, 50 mg on the 2 and 3 day Blood samples (3 mL) will be collected 2, 4, 8, 12 and 24 hours after each dose of caspofungin for 3 consecutive days.

Sponsors & Collaborators

  • Medical University of Lublin

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-05
Primary Completion
2018-08-06
Completion
2018-09-03

Countries

  • Poland

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03399032 on ClinicalTrials.gov