Trial record 2 of 2160 for:
"Kidney Failure"
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
Recruitment status was Active, not recruiting
Sponsor:
Saint Louis VA Medical Center
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
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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
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 June 17, 2013