Actively Recruiting
Samples Procurement for Patients With Colorectal Cancer, Gastric Cancer, and Non-malignant Disease Undergoing Surgery
Led by Renmin Hospital of Wuhan University · Updated on 2022-04-29
1000
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting and storing samples such as blood, normal tissue, and tumor tissue from patients diagnosed with colorectal cancer or gastric cancer. They are also gathering samples from patients with non-malignant gastrointestinal diseases like inflammatory bowel disease, gastric ulcer, hemorrhoids, or hernia. The goal is to create a database that links these samples with clinical information for use in current and future research protocols. Samples are collected during scheduled surgeries that patients are already undergoing as part of their usual care. There is no additional intervention or treatment given as part of this study, so the study does not change the patient's medical care. Patients are grouped based on whether they have colorectal or gastric cancer or non-malignant disease. Participants will provide informed consent before joining the study. The collected samples and clinical data will be confirmed by a pathologist over up to three years. The study involves no extra treatments or procedures beyond the scheduled surgery. Participation lasts through the surgical procedure and sample collection, with ongoing data review and storage for future research. The study runs until December 2026.
CONDITIONS
Brief Title
Samples Procurement for Colorectal Cancer, Gastric Cancer, and Non-malignant Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Any patient diagnosed with colorectal cancer, gastric cancer, or non-malignant disease that requires surgery
- Must be willing and able to provide informed consent
You will not qualify if you...
- Subjects whose other health conditions would prevent safe diagnostic or therapeutic intervention
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo scheduled surgery as part of their normal treatment during which samples are collected for the study.
1 visit (in-person)
Duration - Up to 3 years
Participants are observed after surgery as part of routine care and sample collection does not affect treatment.
Follow-up visits as per routine care
Trial Site Locations
Total: 1 location
1
Department of Gastrointestinal Surgery II, Renmin Hospital of Wuhan University
Wuhan, Hubei, China, 430060
Actively Recruiting
Research Team
T
Tao Fu, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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