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TerminatedNCT00419978Updated Jul 4, 2008

The Significance of Sentinel Node Analysis in Colon Cancer

An interventional study of Colectomy in Colon Cancer, sponsored by Legacy Health System. Terminated at 1 site in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2008-07-04.

Sponsored by Legacy Health System · Not applicable, Interventional, and Treatment

Why this study was terminated
Slow accrural to study.
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Non-randomized
Ages
18 Years to 85 Years
Sex
All
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Study 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.

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Conditions studied

  • Colon Cancer

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In context

Colonic Neoplasms

1,432 studies on the registry are indexed under Colonic Neoplasms; 357 are open to participants now.

This study's enrollment of 24 is below the median of 90 across 1,034 interventional studies indexed under Colonic Neoplasms.

Browse Colonic Neoplasms studies →

Lead sponsor

Legacy Health System is the lead sponsor of 30 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

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
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
24 participants (actual)

Interventions

  • ProcedureColectomy
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Study locations

1 site
  • Legacy Good Samaritan Hospital and Medical Center
    Portland, Oregon 97210, United States
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 4, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00419978
Lead sponsor
Legacy Health System
First posted
Jan 9, 2007
Start date
Jun 2004
Completion
May 2008
Last update
Jul 4, 2008

Study contacts

Mark Whiteford, MD
principal investigator · Legayc Health System
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2008. You cannot join it, but the record below documents what was studied.

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Discussion

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