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Daptomycin at high dose for hemodialysis patient

Pharmacokinetics and safety of high-dose intravenous daptomycin in infected hemodialysis patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016101730345N1
Enrollment
10
Registered
2016-10-30
Start date
2011-08-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Catheter related blood stream infection. Catheter-related bloodstream infection (CRBSI)

Interventions

Patient on hemodialysis (regimen 2/2/3) with suspected CRBSI will be treated with Daptomycin at 10mg/kg immediately after dialysis (2 minutes intravenous infusion). Area under curve for 48h (AUC48h),
Treatment - Drugs

Sponsors

CHU de Poitiers
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion: patients > 18 years, requiring conventional hemodialysis for chronic renal failure hospitalized at the University Hospital of Poitiers (CHU de Poitiers) and presenting a CRBSI. Exclusion: pregnant or breeding women, pneumonia, septic shock (which may affect pharmacokinetic parameters and therefore not represent the principal hemodialysis population); CPK >3ULN; known hypersensitivity to Daptomycin.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pharmacokinetics of Daptomycin at 10 mg/kg after dialysisin conventional hemodialysis in patients with central catheter related infections. Timepoint: 1 week. Method of measurement: Cmax, Cmin, AUC.

Secondary

MeasureTime frame
To evaluate clinical parameters (physical examination, vital signs and temperature) in order to monitor infection evolution and side effects in relation to Daptomycin treatment. Timepoint: 2 weeks. Method of measurement: Cinical examination.

Countries

France

Contacts

Public ContactGuillaume Béraud

CHU de Poitiers

guillaume.beraud@chu-poitiers.fr00549444444

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026