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Search / Trial NCT06145230

A Cross-sectional Survey of Colorectal Cancer Patients in Different Age Groups

Launched by WANG GUIYU · Nov 21, 2023

Trial Information

Current as of July 25, 2025

Recruiting

Keywords

Colorectal Caner Age Group Family History Symptomatic Characteristics Pathologic Features

ClinConnect Summary

This clinical trial is looking to better understand colorectal cancer by comparing patients of different ages. Researchers want to find out how symptoms vary among younger and older patients, if there's a genetic link in families, and how the cancer's characteristics differ based on age. This information could help doctors improve prevention and treatment strategies for colorectal cancer, making them more effective for different age groups.

To participate in this study, you need to be at least 18 years old and have been diagnosed with colorectal cancer that requires surgery. You also need to be willing to take part in the survey. If you decide to join, you'll be asked questions about your experience with the disease. Your involvement could provide valuable insights that might help future patients. If you have any concerns or need more information, the research team is there to support you.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Adults aged 18 years and older with a pathologic diagnosis of colorectal cancer;
  • 2. Undergoing surgical treatment of the primary lesion;
  • 3. Voluntary participation of patients.
  • Exclusion Criteria:
  • 1. Do not agree to participate in the survey or withdraw informed consent
  • 2. Patients did not receive surgical treatment or did not undergo pathologic examination

About Wang Guiyu

Wang Guiyu is a dedicated clinical trial sponsor focused on advancing medical research and innovation. With a commitment to enhancing patient care and outcomes, the organization specializes in the design, implementation, and management of clinical trials across various therapeutic areas. Wang Guiyu leverages a collaborative approach, working closely with healthcare professionals, regulatory bodies, and research institutions to ensure compliance and integrity throughout the research process. By prioritizing ethical standards and patient safety, the sponsor aims to contribute to the development of effective therapies that address unmet medical needs.

Locations

Harbin, Heilongjiang, China

Patients applied

0 patients applied

Trial Officials

Ye Tian, Prof.

Study Chair

Second Affiliated Hospital of Harbin Medical University Ethics Committee

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported