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R&D and clinical application of comprehensive sampling and processing operation platform for gastrointestinal tissue specimens

R&D and clinical application of comprehensive sampling and processing operation platform for gastrointestinal tissue specimens

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034011
Enrollment
Unknown
Registered
2020-06-21
Start date
2021-01-01
Completion date
Unknown
Last updated
2020-06-22

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

Conditions

Gastrointestinal malignancy

Interventions

Experimental Group:Operation platform for comprehensive processing of gastrointestinal tissue specimens
Control Group:Traditional specimen processing

Sponsors

Beijing Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with malignant tumors of stomach and intestine in clinical surgery and need surgical intervention treatment; 2. Unlimited age and gender, physical score ECOG<=2, ASA score <=2, resistant to surgery, normal liver, kidney and bone marrow function; 3. Ability to abide by the plan during the study and sign an informed consent; 4. The patient is willing to follow up and cooperate with the full-time staff to make relevant records.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiopulmonary disease and intolerance to surgery; 2. Patients who are reluctant to bear the risk of surgery and fail to sign the informed consent for surgery; 3. Uncontrollable medical diseases (including unstable angina pectoris, myocardial infarction, cerebrovascular accident within 6 months); 4. Cannot receive general anesthesia or surgical treatment due to other organs in the whole body; 5. Have a history of uncontrolled epilepsy, central nervous system diseases or mental disorders; 6. Women of childbearing age during pregnancy or lactation; 7. Preoperative laboratory examinations clearly identify persons with infectious diseases such as AIDS, syphilis, and hepatitis B; 8. Participate in other clinical trials at the same time.

Design outcomes

Primary

MeasureTime frame
Number of lymph nodes detected;

Countries

China

Contacts

Public ContactZhang Jun

Beijing Friendship Hospital

zhangjun5986@ccmu.edu.cn+86 13811055986

Outcome results

None listed

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