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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01514045
Other study ID # IRB-20285
Secondary ID SU-01172012-8987
Status Recruiting
Phase
First received
Last updated
Start date April 2011
Est. completion date December 2025

Study information

Verified date February 2023
Source Stanford University
Contact Alison Almeda
Phone 650-497-3619
Email GCRegistry@stanford.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Gastric Cancer Registry will combine data acquired directly from patients with gastric cancer; with a family history of gastric cancer in a first or second degree relative; or persons with a known germline mutation in their CDH1 (E-Cadherin) gene via an online questionnaire with genomic data obtained from saliva, blood and tissue samples. The purpose of this registry is to gain better understanding of the causes of gastric cancer, both environmental and genetic; whether certain genomic data can predict outcomes of treatment and survival.


Description:

Collect detailed clinical and epidemiological information on eligible patients via an online registry and a detailed patient questionnaire. Participants can opt in to contribute a blood or saliva sample and paraffin block samples from a previous gastric surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date December 2025
Est. primary completion date May 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients are eligible if they have a histologically proven gastric tumor including gastroesophageal tumors; OR they have a family history of gastric cancer in a first or second degree relative; OR persons with a known germline mutation in their CDH1 (E-Cadherin) gene. 2. 18 years of age or older 3. Adequate English proficiency to complete online consent and questionnaire. Spanish-language proficiency as an alternative to English-language proficiency. Exclusion Criteria: 1. Under 18 years of age 2. No history of gastric cancer or gastric cancer in a family member or a known germline mutation in their CDH1 gene.

Study Design


Related Conditions & MeSH terms


Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Collect detailed clinical and epidemiological information on patients with gastric cancer; with a family history of gastric cancer in a first or second degree relative; or persons with a known germline mutation in their CDH1 (E-Cadherin) gene 1 day
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