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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03972956
Other study ID # SAMPGICUS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 23, 2020
Est. completion date December 23, 2026

Study information

Verified date April 2022
Source Renmin Hospital of Wuhan University
Contact Tao Fu, MD
Phone +8613720120190
Email tfu001@whu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purposes of this study are to collect and store samples including blood, normal and tumor tissue from patients with colorectal cancer or gastric cancer, to collect and store samples including blood and/or normal gastrointestinal tissue (if available) from patients with non-malignant disease (including, but not limited to, inflammatory bowel disease (IBD), gastric ulcer, hemorrhoids or hernia), and to create a database for the collected samples and allow access to relevant clinical information for current and future protocols.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 23, 2026
Est. primary completion date December 23, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Any patient diagnosed with colorectal cancer, gastric cancer, non-malignant disease that requires undergoing surgery. - Must be willing and able to provide informed consent. Exclusion Criteria: - Subjects whose comorbidities would preclude diagnostic or therapeutic intervention.

Study Design


Intervention

Other:
No intervention will be given to patients.
Samples are collected at the time of a scheduled surgery that is part of normal treatment. This study will not have any impact on the care or treatment the patient receives.

Locations

Country Name City State
China Department of Gastrointestinal Surgery II, Renmin Hospital of Wuhan University Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Renmin Hospital of Wuhan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Confirmation of diagnosis by pathologist Once tissue is collected, those samples that have a confirmed diagnosis of disease by the pathologist will be used. Up to 3 years
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