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BIA Versus Physician Adjustment in Acute Kidney Injury Patients Requiring Renal Replacement Therapy

NCT03916861 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2019-04-16

No results posted yet for this study

Summary

This study was designed to compare the efficacy of BIA and physician adjustment to prevent intradialytic hypotension in patients with acute kidney injury who received renal replacement therapy. The investigators randomized 9 patients with acute kidney injury and volume overloaded who underwent acute hemodialysis for 45 sessions in Vajira hospital between October 2017 and February 2018. In physician adjust-group (control) estimate by physical examination and fluid balance record. Primary outcome was intradialytic hypotensive episode and secondary outcome was hemodialysis-related adverse events and other clinical outcome.

Conditions

  • Intradialytic Hypotension
  • Cardiac Event
  • Renal Insufficiency
  • Hospital Length of Stay

Interventions

DEVICE

Bioelectrical Impedance Analysis

We use Inbody S20 analysis to measure fluid status before each hemodialysis session to guide fluid removal.

PROCEDURE

Physician-guided

This intervention used physical examination as guided to adjust fluid therapy together with the chart record of intake and output per day

Sponsors & Collaborators

  • Bangkok Metropolitan Administration Medical College and Vajira Hospital

    lead OTHER_GOV

Principal Investigators

  • Thananda Trakarnvanich · Vajira Hospital ,Navamindradhiraj University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-01
Primary Completion
2018-02-28
Completion
2018-02-28

Countries

  • Thailand

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 NCT03916861 on ClinicalTrials.gov