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Establishment of Gastrointestinal Tumor Organoids Database and Consistency of Organoid Drug Sensitivity Test and Clinical Efficacy of Gastric Cancer

Establishment of Gastrointestinal Tumor Organoids Database and Consistency of Organoid Drug Sensitivity Test and Clinical Efficacy of Gastric Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068378
Enrollment
Unknown
Registered
2023-02-16
Start date
2023-02-13
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Gastrointestinal Tumor

Interventions

Test group:Obtain puncture tissue and conduct organoid drug sensitivity test
Database building group:Obtain puncture tissue and conduct organoid

Sponsors

Beijing Friendship Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Patients with gastrointestinal tumors confirmed by pathology and imaging; 2) The clinical manifestations are the following two types of multi-node samples: a. patients with gastric cancer who have received radical surgery and are currently in remission but have a certain risk of recurrence; b. patients with advanced gastric cancer receiving drug treatment; 3) Complete clinicopathological and follow-up data; 4) The patient voluntarily joins the study and signs the informed consent form, with good compliance and cooperation in follow-up; 5) 18-75-year-old; patients with good general condition can tolerate chemotherapy and targeted treatment;

Exclusion criteria

Exclusion criteria: 1) Failure to comply with the research protocol or research procedure; 2) Have a history of other malignant tumors in the last 5 years; 3) Any unstable systemic disease, including uncontrolled hypertension, unstable angina pectoris, angina pectoris that has begun to attack within the last three months, congestive heart failure (=NYHA Level II), myocardial infarction within six months, serious arrhythmia requiring drug treatment, liver, kidney or metabolic disease); 4) Uncontrolled infection; 5) Patients with mental illness; 6) The researcher believes other conditions that are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Disease free survival;Progression free survival;

Secondary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactZhigang Bai

Beijing Friendship Hospital,Capital Medical University

baizhigang@ccmu.edu.cn13126617140

Outcome results

None listed

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