VolumE maNagement Under Body Composition Monitoring in Critically Ill patientS on CRRT

NCT03330626 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 244

Last updated 2017-11-06

No results posted yet for this study

Summary

Although monitoring fluid balance for continuous renal replacement therapy-treated patients is an important issue, most physicians usually use conventional methods such as the difference between the amount of intake and output (I \& O), which is not objective way. Meanwhile, bioimpedance electrical vector analysis presents the patients' fluid status with more objective data. Thus, the investigators will investigate the clinical benefit for monitoring fluid balance when the investigators use InBody S10, one of representative bioimpedance electrical vector analysis, compared with conventional methods among the patients who need continuous renal replacement therapy.

Conditions

  • Renal Dialysis
  • Fluid Overload

Interventions

DEVICE

InBody group

As one of representative BIVA, it provides the patients' fluid status with more objective data such as TBW, ECW, ICW, etc.

OTHER

IO group

Fluid removal are guided by intake-output balance.

Sponsors & Collaborators

  • Seoul National University Bundang Hospital

    collaborator OTHER
  • SMG-SNU Boramae Medical Center

    collaborator OTHER
  • Ewha Womans University Mokdong Hospital

    collaborator OTHER
  • Seoul National University Hospital

    lead OTHER

Principal Investigators

  • Sejoong Kim, MD,PhD · Department of Internal Medicine, Bundang Seoul National University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-01
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • South Korea

Study Locations

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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 NCT03330626 on ClinicalTrials.gov