Colorectal Cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Histopathologically confirmed colorectal cancer. Prior to screening, participants must be fully informed and provide written informed consent. Aged 18–79 years, with no restrictions on sex. Scheduled to undergo curative (radical) surgical resection. Eastern Cooperative Oncology Group (ECOG) performance status of 0–1.
Exclusion criteria
Exclusion criteria: Individuals with a history of severe allergy to the main ingredients or excipients of probiotic fermented dairy products, or with an allergic constitution. Receipt of any live attenuated vaccine within 30 days prior to the first dose. Inability to swallow the study product normally, or presence of malabsorption syndrome, or other conditions that preclude intestinal absorption of the study product or may interfere with the absorption of GR-3. Known drug abuse or alcohol abuse. Pregnant or breastfeeding women. Any other condition or circumstance that, in the investigator’s judgment, makes the participant unsuitable for enrollment in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abundance of key microbial taxa;Intestinal barrier indicator D-lactate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Inflammatory cytokines;Key metabolites; | — |
Countries
China
Contacts
The Second Hospital of Lanzhou University