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NCT05015296Recruiting

The Impact of Immune Cell Changes During the Perioperative Period on the Prognosis of Patients With Colorectal Cancer

A Multicenter, Prospective, Non-interventional Real-world Study of the Impact of Immune Cell Changes During the Perioperative Period on the Prognosis of Patients With Colorectal Cancer

Source: ClinicalTrials.gov · Last updated 20 Jul 2026

Brief summary (registry, in English)

This is a multi-center, prospective, non-interventional real-world study. In a real-world environment, in line with the current status of the domestic diagnosis and treatment process, and on the premise of not increasing the burden of patients and medical resources, we explore the best indicators for predicting the outcome of patients with Clinical Research Coordinator (CRC) after surgery. The inclusion criteria for patients are perioperative patients with CRC. Real-world data analysis were conducted to determine whether immunization interventions versus non-interventions were able to improve patients' clinical outcomes (OS, PFS).

Status (registry)
Recruiting
Study type
Observational
Enrollment
7000 (estimated)
First submitted
27 Jul 2021
Start date
23 Nov 2021
Primary completion date
30 Jun 2027
Lead sponsor
Beijing Friendship Hospital
NCT number
NCT05015296

What you commit to

  • Study type: Observational
  • Planned participants: 7000
  • From 23 Nov 2021 to the primary completion date, 30 Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • People with a history of psychotropic drug abuse and unable to quit or those with mental disorders;

Other

  • Patients who refused to sign informed consent;
  • Patients complicated with other tumors;
  • Pregnant or lactating women;
  • Postoperative histopathological examinations for patients with non-CRC type;
  • Patients who could not be followed up.

Who the study is looking for

  • 18-85 years old, regardless of gender;
  • Patients with newly diagnosed CRC who are planned to undergo surgery (including patients with metastases but still feasible for surgery);
  • Patients who have not been diagnosed for the first time and have not received surgical treatment and now planned to undergo surgery(e.g., patients after neoadjuvant radiotherapy and chemotherapy for middle and low rectal cancer).

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beijing Frendship Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.