- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01031056
Collection of Biospecimen & Clinical Information in Patients w/ Gastrointestinal Cancers
Collection of Biospecimen and Clinical Information in Patients With Gastrointestinal Cancers
We have an active research program in gastrointestinal cancers including clinical trials, epidemiologic, and translational studies. We would like to establish a biospecimen bank linked to useful clinical information in order to learn more about diagnostic, predictive and prognostic markers for gastrointestinal cancers.
PRIMARY OBJECTIVES:
1. To collect and store tumor and normal tissue (previously collected paraffin embedded or frozen specimen) and blood in patients with gastrointestinal (GI) cancers.
SECONDARY OBJECTIVES:
- Collect detailed clinical information via a patient questionnaire that includes demographic, socioeconomic, lifestyle, family, past medical, medication and cancer histories
- Collect details about the tumor specimen extracted from patient charts.
Study Overview
Status
Conditions
- Gastrointestinal Neoplasms
- Pancreatic Cancer
- Anal Cancer
- Colon/Rectal Cancer
- Hepatobiliary Cancers
- Gastric (Stomach) Cancer
- Gynecologic Cancers
- Gastro-Esophageal(GE) Junction Cancer
- Gynecologic Cancers Cervical Cancer
- Gastrointenstinal Stromal Tumor (GIST)
- Colon/Rectal Cancer Colon Cancer
- Colon/Rectal Cancer Rectal Cancer
- Colon/Rectal Cancer Anal Cancer
- Hepatobiliary Cancers Liver
Intervention / Treatment
Study Type
Contacts and Locations
Study Locations
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California
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Stanford, California, United States, 94305
- Stanford University School of Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:1. Patients are eligible if they have a histologically proven gastrointestinal cancer (esophageal, gastroesophageal junction, gastric, small intestine, appendix, colon, rectum, anus, liver, gallbladder, bile ducts, pancreas, neuroendocrine, and GI stromal tumor).
2. 18 years of age or older
3. Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria:None
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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None: Biospecimen will be collected for future research.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Teri A Longacre M.D., Stanford University
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Neoplasms
- Neoplasms by Site
- Gastrointestinal Diseases
- Stomach Diseases
- Colonic Diseases
- Intestinal Diseases
- Intestinal Neoplasms
- Rectal Diseases
- Anus Diseases
- Stomach Neoplasms
- Colorectal Neoplasms
- Rectal Neoplasms
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Anus Neoplasms
Other Study ID Numbers
- SU-09092009-3840
- GI0004
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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