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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00055848
Other study ID # CALGB-150008
Secondary ID CALGB-150008CDR0
Status Completed
Phase N/A
First received March 6, 2003
Last updated July 12, 2016
Start date December 2001
Est. completion date October 2010

Study information

Verified date July 2015
Source Alliance for Clinical Trials in Oncology
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

RATIONALE: Genetic studies may help in understanding the genetic processes involved in the development of some types of cancer.

PURPOSE: Clinical trial to study the cancer-related genes in patients who have colon cancer or adenomatous polyps.


Description:

OBJECTIVES:

- Identify human colon neoplasia susceptibility genes in patients with colon cancer or adenomatous polyps.

- Correlate the inheritance of novel susceptibility alleles for adenomatous polyposis of the colon with colon neoplasia in these patients.

- Correlate colon neoplasia susceptibility with the presence of COX-2, sPLA2, and DNMT genes in these patients.

- Identify a novel gene that governs increased susceptibility to colon adenoma and cancer in the genome of these patients.


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date October 2010
Est. primary completion date October 2010
Accepts healthy volunteers No
Gender Both
Age group N/A to 70 Years
Eligibility DISEASE CHARACTERISTICS:

- Diagnosis of colon cancer or polyps at age 70 or under

- Has a living full sibling with diagnosis of colon cancer or polyps at age 70 or under

- No history of familial adenomatous polyposis syndrome

- No hereditary nonpolyposis colon cancer, according to Amsterdam criteria

- No known I1370K adenomatous polyposis of the colon susceptibility variant

- Enrolled on 1 of the following clinical trials:

- CLB-9581

- CLB-89803

- CLB-80001 NOTE: Patients do not need to be receiving protocol therapy. Patients who are outside the treatment protocol's follow-up range are eligible. Patients who discontinued therapy for any reason, including toxic effects, are eligible.

PATIENT CHARACTERISTICS:

Age

- 70 and under at diagnosis

Other

- No significant psychiatric illness that would preclude giving informed consent

- No inflammatory bowel disease (in patient or sibling)

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Genetic:
cytogenetic analysis

gene mapping

microarray analysis


Locations

Country Name City State
United States Wayne Memorial Hospital, Incorporated Goldsboro North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Alliance for Clinical Trials in Oncology National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

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