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Effect of Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus Cereus Tablets on Chemotherapy and Radiotherapy of Colorectal Cancer

Effect of Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus Cereus Tablets on Chemotherapy and Radiotherapy of Colorectal Cancer

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040916
Enrollment
Unknown
Registered
2020-12-15
Start date
2020-12-01
Completion date
Unknown
Last updated
2022-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Interventions

experimental group:Orally take Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus cereus Tablets

Sponsors

The Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Informed consent; 2.Preoperative pathological diagnosis of colorectal cancer; 3.Patients who need postoperative radiotherapy and chemotherapy after partial colorectal resection; 4.The patients were in good condition, aged 40-70 years.

Exclusion criteria

Exclusion criteria: 1. The patients had severe heart, lung, kidney, liver dysfunction and metabolic diseases; 2. Distant metastasis detected; 3. Those who are allergic to Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus cereus Tablets; 4. The patient had no serious complications before the operation and had not received radiotherapy or chemotherapy; 5. Those who have immune disease, cannot take orally or absorb digestive tract drugs or are allergic to probiotics; 6. Pregnant and lactating women; 7. During the study period, it may be necessary to use drugs prohibited by clinical trial protocol, such as antibiotics and other drugs affecting intestinal flora; 8. Patients with autoimmune disease, immunodeficiency disease, or history of organ transplantation; 9. Participate in clinical trials of other anti-tumor drugs within 30 days before enrollment; 10. Patients who were considered unsuitable for this study were considered by the researchers.

Design outcomes

Secondary

MeasureTime frame
High throughput sequencing of feces;Metabolomics of feces;High throughput sequencing of intestinal juice;Metabolomics of intestinal juice;Blood routine;Liver function tests;Renal function tests;

Countries

China

Contacts

Public ContactDeng Xiaorong

The Second Affiliated Hospital of Nanchang University

dengxr77@163.com+86 13870889003

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026