Skip to main content
MedPath Trial logoMedPath TrialMedPath Trial Home
Clinical Trials/NCT01405092
NCT01405092CompletedNot Applicable

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

Dallas VA Medical Center2 sites in 1 country28 target enrollmentStarted: April 2010Last updated:
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
28
Locations
2
Primary Endpoint
compare number of hypotensive events in treatment versus control arms
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study 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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Fed
Responsible Party
Principal Investigator
Principal Investigator

Devasmita C. Dev MD

Director of In-center and Home Dialysis

Dallas VA Medical Center

Study Sites (2)

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