Suspended

NIPCONNon-Invasive Prediction of Colorectal Neoplasia

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What is being collected

Data Collection

Collected from today forward - Prospective
DNA Samples
Who is being recruted

Adenoma+22

+ Colonic Diseases

+ Digestive System Diseases

From 18 to 85 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: August 2006
See protocol details

Summary

Principal SponsorCorporal Michael J. Crescenz VA Medical Center
Last updated: September 27, 2016
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2006

Actual date on which the first participant was enrolled.

The primary objectives is to test the efficacy of Adnab-9 stool testing in a population at high-risk for colorectal neoplasia and directly compare it to that of the FOBT and secondarily, identify the source of the Adnab-9 antigen to determine influences of diet and environment on its expression. The design is a prospective cross sectional (Part 1) and a case-control longitudinal follow-up study (Part 2) using a brief questionnaire to assess risk for cancer in a total of 2800 Part I patients will be enrolled designed to achieve a database of high risk individuals and measure fecal Adnab-9 levels before a clinically indicated colonoscopy is performed. The patients submit 4 FOBT cards in a routine manner by mail, 3 are used for the FOBT and stool is extracted from the last card for the Adnab-9 ELISA which is reported as OD/5ug protein/well. 100 Part 2 enrollees are then selected on the basis of positive fecal Adnab-9 test candidates matched with a like number of patients with negative stool results who have had their initial colonoscopy and who will have a 5-year follow-up colonoscopy. Detailed Adnab-9 testing (immunohistochemical Adnab-9 binding; blood biomarker estimations and Adnab-9 Western blotting) will be performed on various bodily fluids to perfect the method of testing and completion of the detailed questionnaire to check for reproducibility and interim lifestyle changes in these participants.

NCT01815463
Principal SponsorCorporal Michael J. Crescenz VA Medical Center
Last updated: September 27, 2016
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

2282 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 85 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

AdenomaColonic DiseasesDigestive System DiseasesDigestive System NeoplasmsGastrointestinal DiseasesGastrointestinal NeoplasmsIntestinal DiseasesIntestinal NeoplasmsIntestinal PolypsCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Glandular and EpithelialNeoplastic Syndromes, HereditaryPolypsRectal DiseasesPathological Conditions, Signs and SymptomsAdenomatous PolypsPathological Conditions, AnatomicalGenetic Diseases, InbornIntestinal PolyposisColonic PolypsAdenomatous Polyposis ColiColorectal Neoplasms

Criteria

3 inclusion criteria required to participate
ability to complete a consent form

must be at above average risk for colorectal neoplasia

physically able to undergo colonoscopy or barium enema

5 exclusion criteria prevent from participating
Low risk for colorectal neoplasia

Mentally handicapped

Physically infirm

Pregnant individuals

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Philadelphia VAMC

Philadelphia, United StatesOpen Philadelphia VAMC in Google Maps
SuspendedOne Study Center