NCT00419978

Brief Summary

This study is for the patient with colon cancer, who is going to have colon cancer surgery. The purpose of this research study is to examine a specific lymph node, called the sentinel node. Lymph nodes are located throughout your body and cancer may spread by means of those lymph nodes. The sentinel node is the one located closest to your tumor. This study will find out if examining the sentinel node can help to predict disease progression. Since the value of this exam is unknown, taking part in this study will not change your clinical care.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2004

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2004

Completed
2.6 years until next milestone

First Submitted

Initial submission to the registry

January 5, 2007

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 9, 2007

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2008

Completed
Last Updated

July 4, 2008

Status Verified

June 1, 2008

First QC Date

January 5, 2007

Last Update Submit

June 27, 2008

Conditions

Colon Cancer

Interventions

ColectomyPROCEDURE

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • All patients must consent to participate in study
  • Patients will be tracked for five years
  • A blood test (CEA) will be collected every six months
  • A CT scan will be performed annually
  • A colonoscopy will be performed at 1 and 5 years post-surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Legacy Good Samaritan Hospital and Medical Center

Portland, Oregon, 97210, United States

Location

Related Links

MeSH Terms

Conditions

Colonic Neoplasms

Interventions

Colectomy

Condition Hierarchy (Ancestors)

Colorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal Diseases

Intervention Hierarchy (Ancestors)

Surgical Procedures, ColorectalDigestive System Surgical ProceduresSurgical Procedures, Operative

Study Officials

  • Mark Whiteford, MD

    Legayc Health System

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 5, 2007

First Posted

January 9, 2007

Study Start

June 1, 2004

Study Completion

May 1, 2008

Last Updated

July 4, 2008

Record last verified: 2008-06

Locations

US(1)