Citrate Anticoagulation for Postdilution Hemofiltration

NCT03969966 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2020-05-11

No results posted yet for this study

Summary

This study evaluates a protocol for regional citrate anticoagulation in critically ill patients with acute kidney injury who are treated with continuous veno-venous haemofiltration in postdilution mode.

Conditions

Interventions

OTHER

renal replacement therapy as clinically indicated

Continuous renal replacement therapy

Sponsors & Collaborators

  • Diamed GmbH, Cologne, Germany

    collaborator UNKNOWN
  • Heinrich-Heine University, Duesseldorf

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-14
Primary Completion
2020-12-31
Completion
2021-07-31

Countries

  • Germany

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 NCT03969966 on ClinicalTrials.gov