NCT00851851

Completed

New Non-invasive Methods for Real-time Monitoring of Organ F...

Washington University School of Medicine Source

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Other study identifiers

Sponsor study identifier

201110033

Study Type

observational

Actual enrollment (reported)

641

Locations

1 country

Sites

1

Timeline

Study Start

January 2009

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2015

Actual (reported)

Study Completion

June 2016

Actual (reported)

Brief Summary

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

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 641 participants
Study completion date: June 2016
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2009
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
February 25, 2009
Actual (reported)
First Posted
February 26, 2009
Actual (reported)
Primary Completion
December 2015
Actual (reported)
Study Completion
June 2016
Actual (reported)

Last Updated: July 20, 2016
Status Verified: July 2016
Last Update Submitted: July 18, 2016

Conditions

Acute Renal Failure Chronic Renal Failure

Keywords

Surgical patients

Outcome Measures

Primary Outcomes (1)

To identify acute, chronic or lack of renal failure
Pre-op, intraoperative, post operatively (1-6 months)

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodProbability Sample

Study Population

Surgical patients.

You may qualify if:

Patients \> 18 years of age

You may not qualify if:

Sponsors & Collaborators

Washington University School of Medicine
Otherlead

Study Sites (1)

Barnes Jewish Hospital

St Louis, Missouri, 63110, United States

Biospecimen

Retention: SAMPLES WITH DNA

Urine and blood samples

MeSH Terms

Conditions

Acute Kidney InjuryKidney Failure, Chronic

Condition Hierarchy (Ancestors)

Renal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesRenal Insufficiency, ChronicChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

Jerry Morrissey, PhD
Washington University School of Medicine
PRINCIPAL INVESTIGATOR

Enrollment

641 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE ONLY
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

February 25, 2009

First Posted

February 26, 2009

Study Start

January 2009

Date type not reported

This date has not been verified as actual or estimated.

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Vasodilators and Anti-Oxidant Therapy in Early ATN

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NCT01907061

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Not ApplicableCompleted

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

Contact the study team to confirm eligibility.

Primary Completion

December 2015

Actual (reported)

Study Completion

June 2016

Actual (reported)

Last Updated

July 20, 2016

Record last verified: 2016-07

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00851851
Data provider: ClinicalTrials.gov
Source updated: 2016-07-20
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:40:46 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Biospecimen

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations