Metabolomics-Based Detection of Colorectal Cancer
Completed
Conditions studied: Colorectal Cancer
In brief
The purpose of this study is to collect specimens to perform metabolic profiling of serum and urine from patients with colorectal cancer, colon polyps and healthy patients.
Key facts
- Study ID
- NCT00507598
- Run by
- Indiana University
- People needed
- 69
- Starts
- 2007-07-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2014-09-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients with resectable colorectal cancer must have samples collected (serum/urine) prior to surgery and/or after surgery, but prior to starting chemotherapy.
- Patients with metastatic colorectal cancer must have samples collected prior to initiating chemotherapy, and after chemotherapy initiation: every 3 months for up to 24 months.
- Subjects must be ≥ 18 years of age.
- Subjects undergoing screening colonoscopy are able to participate as healthy controls or as patients with colon polyps if colonoscopy identifies colon polyps being present (informed consent will be signed first and samples will be collected; after colonoscopy the samples will be identified as "healthy" or "polyps").
- For patients who underwent biopsy or surgery for colorectal cancer, enough tissue needs to be available for testing, as appropriate per patients groups in the protocol Schema.
- Subjects must be able to attend follow up or treatment visits per investigator's recommendations for up to 24 months for collection of serum/urine specimens.
- Female patients known to be pregnant are not eligible for this protocol.
- Subjects must be able to undergo an 8-hr overnight fast prior to metabolomic testing
You may not qualify if…
- Presence of an invasive cancer other than colorectal cancer is an exclusion criterion
Where it is running
- Indiana University Cancer Center — Indianapolis, Indiana, United States
Full record on ClinicalTrials.gov
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