New Non-invasive Methods for Real-time Monitoring of Organ Function. (RTMKF)

This study has been completed.

Sponsor:

Information provided by (Responsible Party):

Washington University School of Medicine

ClinicalTrials.gov Identifier:

NCT00851851

First received: February 25, 2009

Last updated: July 18, 2016

Last verified: July 2016

History of Changes

Purpose

Measuring novel proteins in the urine of surgical patients that can be used to diagnose impending acute or chronic renal failure.

Condition
Acute Renal Failure Chronic Renal Failure


Study Type:	Observational
Study Design:	Observational Model: Case-Only Time Perspective: Prospective
Official Title:	New Non-invasive Methods for Real-time Monitoring of Organ Function.

Resource links provided by NLM:

MedlinePlus related topics: Kidney Failure

U.S. FDA Resources

Further study details as provided by Washington University School of Medicine:

Primary Outcome Measures:

To identify acute, chronic or lack of renal failure [ Time Frame: Pre-op, intraoperative, post operatively (1-6 months) ] [ Designated as safety issue: No ]

Biospecimen Retention: Samples With DNA

Urine and blood samples


Enrollment:	641
Study Start Date:	January 2009
Study Completion Date:	June 2016
Primary Completion Date:	December 2015 (Final data collection date for primary outcome measure)

Eligibility


Ages Eligible for Study:	18 Years and older (Adult, Senior)
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No
Sampling Method:	Probability Sample

Study Population

Surgical patients.

Criteria

Inclusion Criteria:

Patients > 18 years of age

Exclusion Criteria:

Patients at end stage renal disease
Patients dependent on dialysis at time of surgery

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: NCT00851851

Locations


United States, Missouri
Barnes Jewish Hospital
St. Louis, Missouri, United States, 63110

Sponsors and Collaborators

Washington University School of Medicine

Investigators


Principal Investigator:	Jerry Morrissey, PhD	Washington University School of Medicine

More Information


Responsible Party:	Washington University School of Medicine
ClinicalTrials.gov Identifier:	NCT00851851 History of Changes
Other Study ID Numbers:	201110033
Study First Received:	February 25, 2009
Last Updated:	July 18, 2016
Health Authority:	United States: Institutional Review Board

Keywords provided by Washington University School of Medicine:


Surgical patients

Additional relevant MeSH terms:


Renal Insufficiency Kidney Failure, Chronic Acute Kidney Injury	Kidney Diseases Urologic Diseases Renal Insufficiency, Chronic

ClinicalTrials.gov processed this record on September 23, 2016

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