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NCT01031056 Clinical Trial

Collection of Biospecimen & Clinical Information in Patients w/ Gastrointestinal Cancers

Pancreatic Cancer Clinical Trial

Official title:
Collection of Biospecimen and Clinical Information in Patients With Gastrointestinal Cancers

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01031056
Other study ID # SU-09092009-3840
Secondary ID GI0004
Status Withdrawn
Phase N/A
First received December 10, 2009
Last updated May 24, 2012
Start date January 2010
Est. completion date January 2099

Study information
Verified date May 2012
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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:

1. Collect detailed clinical information via a patient questionnaire that includes demographic, socioeconomic, lifestyle, family, past medical, medication and cancer histories

2. Collect details about the tumor specimen extracted from patient charts.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 2099
Est. primary completion date January 2099
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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 Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• Blood Draw

• Frozen Tumor Specimens

Locations
Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (3)
Lead Sponsor Collaborator
Stanford University Caring for Carcinoid Foundation, GI Cancer Research Gift Fund

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary None: Biospecimen will be collected for future research. No
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