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Elimination of Antibiotics During Citrate-anticoagulated Continuous-veno-venous-haemodialysis

Elimination of Antibiotics During Citrate-anticoagulated Continuous-veno-venous-haemodialysis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02533609
Acronym
DIADSORBMAB
Enrollment
30
Registered
2015-08-27
Start date
2015-09-30
Completion date
2020-12-31
Last updated
2020-05-11

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

Conditions

Acute Kidney Injury, Bacterial Infection

Brief summary

Acute kidney injury (AKI) requiring renal replacement therapy is common in critically ill patients. The major causes of AKI are severe sepsis and septic shock requiring effective antibiotic treatment. Patients with sepsis on ICUs usually are haemodynamically instable so that renal replacement therapy is applied using continuous techniques. In recent years, the efficacy of renal replacement therapies has improved, namely by using regional citrate anticoagulation which improves filter lifetime and filter patency. At present, the extent of removal of antibiotic drugs using citrate-anticoagulated CVVHD in critically ill patients has not been investigated thoroughly. Thus, the investigators want to investigate 1. whether and to what extent antibiotic drugs (piperacillin/tazobactam and imipenem/cilastatin) are removed during citrate-anticoagulated CVVHD per se 2. whether filter patency during citrate-anticoagulated CVVD remains stable during a treatment period of 72 h

Interventions

None listed

Sponsors

Fresenius Medical Care Deutschland GmbH
CollaboratorINDUSTRY
Heinrich-Heine University, Duesseldorf
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Intensive care patients with acute kidney injury requiring continous renal replacement therapy with citrate-anticoagulation * Age \> 18 y

Exclusion criteria

* \< 18 y * Pregnancy * Contraindications against citrate-anticoagulation or continous renal replacement therapy

Design outcomes

Primary

MeasureTime frameDescription
Removal of antibiotic drugs during day 1 - 2 - 3 of citrate anticoagulated CVVHD (mg/d)up to three daysTotal hemofilter clearance (ml/min) of imipenem/cilastatin and piperacillin/tazobactam on each treatment day during an 8-hour dosing interval using blood sided clearance \- Total amount of antibiotic drug which is eliminated via the filter during 24 h using filter clearance and delivered dialysis dose during 24 h
Filter patency during day 1 - 2 - 3 of citrate anticoagulated CVVHDup to three daysFilter patency is calculated as a function of the sieving coefficient for small solutes (i.e. creatinine and the respective antibiotic drugs) over the first 72 h, Sieving coefficient is without dimension

Countries

Germany

Outcome results

None listed

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