- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02034448
CRRTNet Registry- A Prospective Observational Registry (CRRT)
January 12, 2015 updated by: AKI Critical Care Research Foundation
CRRTNet Outcome Registry
An observational registry to monitor the outcome of CRRT in adults with acute kidney injury.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Observational
Enrollment (Anticipated)
2000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Michigan
-
Ann Arbor, Michigan, United States, 48109
- Recruiting
- Mike Heung
-
Contact:
- Mike Heung, MD
- Phone Number: 734-936-4890
- Email: mheung@umich.edu
-
Principal Investigator:
- Mike Heung, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
This is a prospective observational registry.
A minimum sample size of 2000 patients with the detailed information being obtained would embody the largest and most detailed repository of adult CRRT patient information available.
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Acute Kidney Injury
CRRT intervention with adult patients with Acute Kidney Injury
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Mortality
Time Frame: 30 days
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Length of Stay
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Mike Heung, MD, University of Michigan Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2013
Primary Completion (Anticipated)
December 1, 2018
Study Completion (Anticipated)
December 1, 2018
Study Registration Dates
First Submitted
January 10, 2014
First Submitted That Met QC Criteria
January 10, 2014
First Posted (Estimate)
January 13, 2014
Study Record Updates
Last Update Posted (Estimate)
January 14, 2015
Last Update Submitted That Met QC Criteria
January 12, 2015
Last Verified
January 1, 2015
More Information
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Fujian Provincial HospitalRecruitingContinuous Renal Replacement Therapy | Regional Citrate Anticoagulation | Renal InjuryChina
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Clinical Trials on Continuous Renal Replacement Therapy
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-
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Chulalongkorn UniversityCompletedAcute Renal FailureThailand
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Sunnybrook Health Sciences CentreDialysis Solutions Inc.Completed
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Southeast University, ChinaCompletedRespiratory Failure With HypercapniaChina
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Chulalongkorn UniversityCompleted
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University of ThessalyRecruitingSepsis | Septic Shock | Renal Replacement Therapy | Aminoglycoside ToxicityGreece