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Impact of Early Renal Involvement on the Development of Severe In-hospital Renal Failure (EARLI)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified July 2009 by Saint Louis VA Medical Center.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00806039
First Posted: December 10, 2008
Last Update Posted: July 16, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Saint Louis VA Medical Center
  Purpose
The purpose of this study is to determine whether renal team involvement early at the onset of kidney injury will prevent further developement of more severe renal failure and worse hospitalization outcomes.

Condition Intervention
Kidney Failure, Acute Renal Insufficiency, Acute Kidney Failure Renal Insufficiency Other: Early Renal Involvement

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Impact of EArly Renal Involvement on the Developement of Severe In-hospital Renal Failure

Resource links provided by NLM:


Further study details as provided by Saint Louis VA Medical Center:

Primary Outcome Measures:
  • Severe renal Failure [ Time Frame: 10 days ]

Secondary Outcome Measures:
  • Composite outcome morbidity mortality [ Time Frame: hospitalization ]

Estimated Enrollment: 300
Study Start Date: December 2008
Estimated Study Completion Date: July 2009
Estimated Primary Completion Date: July 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1
Early renal involvement
Other: Early Renal Involvement
Renal Consultation
No Intervention: 2
control

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Hospitalized, elevation in creatinine meeting definition

Exclusion Criteria:

  • CDK5, ESRD,solid organ transplant
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00806039


Locations
United States, Missouri
Saint Louis VA Medical Center
Saint Louis, Missouri, United States, 63106
Sponsors and Collaborators
Saint Louis VA Medical Center
Investigators
Study Director: Tarek M El-Achkar, MD Saint Louis VA Medical Center
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Tarek El-Achkar, MD, Saint Louis VA Medical Center
ClinicalTrials.gov Identifier: NCT00806039     History of Changes
Other Study ID Numbers: 1143004
First Submitted: December 9, 2008
First Posted: December 10, 2008
Last Update Posted: July 16, 2009
Last Verified: July 2009

Keywords provided by Saint Louis VA Medical Center:
Kidney Failure, Acute
Renal Insufficiency, Acute
Kidney Failure
Renal Insufficiency

Additional relevant MeSH terms:
Renal Insufficiency
Acute Kidney Injury
Kidney Diseases
Urologic Diseases