NCT01538810

Completed

Biomarker Correlates of Radiologic Imaging

Washington University School of Medicine Source

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Other study identifiers

Sponsor study identifier

201201061

Study Type

observational

Actual enrollment (reported)

751

Locations

1 country

Sites

1

Timeline

Study Start

February 2012

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

May 2016

Actual (reported)

Study Completion

May 2016

Actual (reported)

Brief Summary

The purpose of this study is to assemble a collection of urine and blood samples for the development and validation of biomarkers potentially useful in correlating or improving the diagnostic utility of abdominal imaging.

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): 751 participants
Study completion date: May 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
February 2012
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
February 20, 2012
Actual (reported)
First Posted
February 24, 2012
Actual (reported)
Primary Completion
May 2016
Actual (reported)
Study Completion
May 2016
Actual (reported)

Last Updated: June 17, 2016
Status Verified: June 2016
Last Update Submitted: June 16, 2016

Conditions

Abdominal CT Imaging Performed as Standard of Care

Keywords

CT imaging

Outcome Measures

Primary Outcomes (1)

Quantitative measures
Confirm the ability of quantitative measure of AQP-1 and ADFP by ELISA from urine and blood samples to develop and validate an assay for patients with renal cancer.
at enrollment

Secondary Outcomes (1)

differentiation of cancerous from non-cancerous renal mass
at analysis

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

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

Sampling MethodNon-Probability Sample

Study Population

Anyone undergoing an abdominal image, meeting eligibility criteria.

You may qualify if:

years and older

Sponsors & Collaborators

Washington University School of Medicine
Otherlead

Study Sites (1)

Washington University School Of Medicine

St Louis, Missouri, 63110, United States

Study Officials

Jerry Morrissey, PhD
Washington University School of Medicine
PRINCIPAL INVESTIGATOR

Enrollment

751 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: ECOLOGIC OR COMMUNITY
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

February 20, 2012

First Posted

February 24, 2012

Study Start

February 2012

Date type not reported

This date has not been verified as actual or estimated.

Undergoing abdominal CT imaging (standard of care)

Signed, informed consent

You may not qualify if:

Patients on dialysis

Contact the study team to confirm eligibility.

Primary Completion

May 2016

Actual (reported)

Study Completion

May 2016

Actual (reported)

Last Updated

June 17, 2016

Record last verified: 2016-06

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: NCT01538810
Data provider: ClinicalTrials.gov
Source updated: 2016-06-17
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:38:02 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)

Secondary Outcomes (1)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations