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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02034448
Other study ID # CRRTNet
Secondary ID
Status Recruiting
Phase N/A
First received January 10, 2014
Last updated January 12, 2015
Start date November 2013
Est. completion date December 2018

Study information

Verified date January 2015
Source AKI Critical Care Research Foundation
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

An observational registry to monitor the outcome of CRRT in adults with acute kidney injury.


Description:

Continuous Renal Replacement Therapy (CRRT) is a form of dialysis provided to critically ill patients with acute renal failure, now known as acute kidney injury (AKI). While we have extensive experience with this therapy in critically ill patients, there is no consensus on when to start CRRT or a clinical standard as to the best possible way to deliver the therapy. Previous studies have examined one aspect of CRRT in detail (for instance the dose of delivered therapy, or anticoagulation strategies) or have been small single center studies, or large multinational studies examining very basic practice patterns. This is a prospective observational cohort study. All patients who receive CRRT as part of their standard of local care will be eligible for the study.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 89 Years
Eligibility Inclusion Criteria: Patients initiating CRRT c. Age > 18 years of age and <89 year of age -

Exclusion Criteria: ? 18 years of age and > 89 year of age

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Continuous Renal Replacement Therapy

Intervention

Procedure:
Continuous Renal Replacement Therapy


Locations

Country Name City State
United States Mike Heung Ann Arbor Michigan

Sponsors (1)

Lead Sponsor Collaborator
AKI Critical Care Research Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality 30 days No
Secondary Length of Stay 6 months No
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