Skip to main content
MedPathMedPath Home
Clinical Trials/NCT01405092
NCT01405092
Completed
Not Applicable

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

Dallas VA Medical Center1 site in 1 country28 target enrollmentApril 2010
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsContinuous Renal Replacement Therapy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Continuous Renal Replacement Therapy
Sponsor
Dallas VA Medical Center
Enrollment
28
Locations
1
Primary Endpoint
compare number of hypotensive events in treatment versus control arms
Status
Completed
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

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

Registry
clinicaltrials.gov
Start Date
April 2010
End Date
August 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Devasmita C. Dev MD

Director of In-center and Home Dialysis

Dallas VA Medical Center

Eligibility Criteria

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

Outcomes

Primary Outcomes

compare number of hypotensive events in treatment versus control arms

Time Frame: 24 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

Study Sites (1)

Loading locations...

Similar Trials

Unknown
Not Applicable
VolumE maNagement Under Body Composition Monitoring in Critically Ill patientS on CRRTRenal DialysisFluid Overload
NCT03330626Seoul National University Hospital244
Completed
Phase 1
Cefiderocol Plasma Concentrations in Patients Receiving Renal Replacement TherapyPharmacokinetics
NCT05373615Hartford Hospital14
Completed
Not Applicable
Study Comparing Dryweight Determination in Hemodialysis Patients With Two MethodsChronic Kidney Disease
NCT02348996Ana Elizabeth Prado Lima Figueiredo57
Completed
Not Applicable
Hemodynamic Monitoring With Mixed Venous SaturationCritically Ill
NCT00303043Policlinico Hospital30
Completed
Not Applicable
sefulness of the Clearsight system for hemodynamic management in patients undergoing total knee arthroplasty
JPRN-UMIN000021678Department of Anesthesiology, Osaka City University Graduate School of Medicine40