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NCT01048281 Clinical Trial

Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

Esophageal Cancer Clinical Trial

Official title:
Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01048281
Other study ID # GIUPR0001
Secondary ID 76274CA109190SU-
Status Recruiting
Phase
First received
Last updated
Start date August 2002
Est. completion date January 2099

Study information
Verified date November 2023
Source Stanford University
Contact Meredith Mills
Phone (650) 724-5223
Email bluett@stanford.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our research of the biology of upper gastrointestinal cancers involves the study of tissue samples and cells from biopsies of persons with gastric or esophageal cancer or blood samples from upper gastrointestinal cancer patients and persons at high inherited risk for these cancers. We hope to learn the role genes and proteins play in the development of gastric and esophageal cancer.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date January 2099
Est. primary completion date January 2099
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Over 18 2. Diagnosed with gastric or esophageal cancer OR at an increased hereditary risk for upper GI cancer Exclusion Criteria: 1. Under 18 2. No family or personal history of gastric or esophageal cancer

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Blood draw

• Tissue tumor biopsy

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

Sponsors (2)
Lead Sponsor Collaborator
Stanford University National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary p53 activity by routine pathologic analysis time of collection
Primary NER activity by routine pathologic analysis time of collection
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