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Continuous Versus Conventional Volume Management During CRRT (Continuous Renal Replacement Therapy)

Not Applicable
Completed
Conditions
Continuous Renal Replacement Therapy
Interventions
Device: use of continuous renal replacement machine for renal replacement
Device: use of blood volume monitoring device in conjunction with machine used for continuous renal replacement to assess and determine volume removal
Registration Number
NCT01405092
Lead Sponsor
Dallas VA Medical Center
Brief Summary

Use of on-line blood volume monitoring during continuous renal replacement therapy can improve volume management in acute kidney injury patients requiring renal replacement

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
28
Inclusion Criteria
  • Patients with kidney injury requiring continuous renal replacement therapy and volume removal
Exclusion Criteria
  • unable to provide or obtain patient consent
  • not expected to survive 48 hours

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Standard volume managementuse of continuous renal replacement machine for renal replacementpatients on this arm will receive usual care volume management during continuous renal replacement therapy
continuous volume managementuse of continuous renal replacement machine for renal replacementuse of Critline, Hemametrics USA, in conjunction with continuous renal replacment therapy to determine volume removal
continuous volume managementuse of blood volume monitoring device in conjunction with machine used for continuous renal replacement to assess and determine volume removaluse of Critline, Hemametrics USA, in conjunction with continuous renal replacment therapy to determine volume removal
Primary Outcome Measures
NameTimeMethod
compare number of hypotensive events in treatment versus control arms24 hour for each arm

compare the number of hypotensive events during use of crit-line monitor over 24 hour period versus during control 24 hour period

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Dallas VA Medical Center

🇺🇸

Dallas, Texas, United States

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