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PHARMACOKINETICS OF CEFEPIME AFTER INTRAPERITONEAL ADMINISTRATION VIA CYCLER-THERAPY IN APD PATIENTS WITHOUT PERITONITIS

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-509930-21-00
Acronym
2
Enrollment
8
Registered
2024-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

CKD 5, Peritoneal Dialysis

Brief summary

AUC, Cmax, Half-life (t1/2), Time to reach maximum drug concentration (tmax)

Detailed description

Ratios of AUC and Cmax of different compartments, Time above the minimal inhibitory concentration T>MIC, Ratio of AUC from 0 to 24 hours (AUC 0-24)/MIC

Interventions

DRUGCefepim-MIP 1 g Pulver zur Herstellung einer Injektions- / Infusionslösung

Sponsors

Noe LGA Gesundheit Region Mitte GmbH
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
AUC, Cmax, Half-life (t1/2), Time to reach maximum drug concentration (tmax)

Secondary

MeasureTime frame
Ratios of AUC and Cmax of different compartments, Time above the minimal inhibitory concentration T>MIC, Ratio of AUC from 0 to 24 hours (AUC 0-24)/MIC

Countries

Austria

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026