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Daptomycin Pharmacokinetics in Critically Ill Patients Undergoing Continuous Veno-venous Hemodiafiltration, a Dose Finding Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01212432
Enrollment
15
Registered
2010-09-30
Start date
2009-12-31
Completion date
2010-03-31
Last updated
2010-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gram-Positive Bacterial Infections

Keywords

Gram positive infection and CRRT

Brief summary

Daptomycin kinetics in CRRT * Trial with medicinal product

Interventions

DRUGDaptomycin

Daptomycin kinetics in CRRT

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* male or female of 18 years or older * females: negative pregnancy test * Hospitalisation in the medical ICU * High suspicion or evidence of Gram-positive infections requiring antibiotic therapy * Subjects receiving standard antibiotic treatment for Gram-positive infection * Evidence of renal failure * Clinical necessity for continuous renal replacement therapy * Written informed consent signed by the patient or a next of kin and an independent physician in case the patient is not able to sign.

Exclusion criteria

* Skeletal muscle disorders or CPK levels of \> 2 x ULN * History of hypersensitivity to the drug * Participation in another study * Subjects with a history of muscle disease * Patients with severe liver function impairment (Child * Life expectancy of less than 5 days

Design outcomes

Primary

MeasureTime frame
Pharmacokinetics2011

Countries

Switzerland

Contacts

Primary Contact01 Studienregister MasterAdmins
+41 (0)44 255 11 11

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026