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

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2009 by Saint Louis VA Medical Center.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Saint Louis VA Medical Center
ClinicalTrials.gov Identifier:
NCT00806039
First received: December 9, 2008
Last updated: July 14, 2009
Last verified: July 2009
  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: Open Label
Primary Purpose: Prevention
Official Title: Impact of EArly Renal Involvement on the Developement of Severe In-hospital Renal Failure

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

Primary Outcome Measures:
  • Severe renal Failure [ Time Frame: 10 days ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Composite outcome morbidity mortality [ Time Frame: hospitalization ] [ Designated as safety issue: No ]

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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Hospitalized, elevation in creatinine meeting definition

Exclusion Criteria:

  • CDK5, ESRD,solid organ transplant
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided by Saint Louis VA Medical Center

Additional 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
Study First Received: December 9, 2008
Last Updated: July 14, 2009
Health Authority: United States: Federal Government

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

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

ClinicalTrials.gov processed this record on July 22, 2014