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Effect of oral probiotic compound preparation for postoperative recovery of gastric cancer

Effect of oral probiotic compound preparation for postoperative recovery of gastric cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022506
Enrollment
Unknown
Registered
2019-04-14
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-04-15

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

Conditions

gastric cancer

Interventions

Experimental group:Oral probiotic compound preparation
Control group:Placebo

Sponsors

Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Informed consent; 2. Pathological diagnosis of gastric cancer; 3. Patients are generally in good condition, aged 18-70 years.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, lung, kidney, liver dysfunction and metabolic diseases; 2. Discovery of distant metastasis; 3. Allergies to probiotics; 4. No serious complications before surgery, no radiation or chemotherapy. 5. Those who have immune diseases, cannot take orally or absorb digestive tract drugs or are allergic to probiotics.

Design outcomes

Primary

MeasureTime frame
High throughput sequencing of feces;—

Countries

China

Contacts

Public ContactDeng xiaorong

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