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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00419978
Other study ID # 750040399
Secondary ID
Status Terminated
Phase N/A
First received January 5, 2007
Last updated June 27, 2008
Start date June 2004
Est. completion date May 2008

Study information

Verified date June 2008
Source Legacy Health System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Terminated
Enrollment 24
Est. completion date May 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- 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

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Colectomy


Locations

Country Name City State
United States Legacy Good Samaritan Hospital and Medical Center Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
Legacy Health System

Country where clinical trial is conducted

United States, 

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