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The post-operation relapse and metastasis of traditional Chinese medicine for patients with upper gastrointestinal cancer intervention study

The post-operation relapse and metastasis of traditional Chinese medicine for patients with upper gastrointestinal cancer intervention study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-POC-16009334
Enrollment
Unknown
Registered
2016-10-08
Start date
2016-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Upper gastrointestinal cancer

Interventions

Chinese traditional medicine group:Traditional Chinese medicine
Chinese traditional medicine group:Support therapy
Chemotherapy group:Standard chemotherapy regimens
Chemotherapy group:Support therapy

Sponsors

China Academy of Chinese Medical Sciences Xiyuan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects eligible for enrollment must meet all of the following criteria: 1. Men or women aged 18 years or older; 2. Provide signed informed consent. The subject is capable of understanding and complying with parameters as outlined in the protocol and able to sign informed consent; 3. Diagnosis of adenocarcinoma of the stomach, T2 or T3 or T4, N0 or N1 or N2 or N3 (Diagnosis Criteria for Primary Gastric Cancer, WS 316-2010), - low 1/3 location(antrum and pylori); No evidence of other distant metastasis; 4. Patients have undergone radical resection of gastric cancer within 6-8 months.

Exclusion criteria

Exclusion criteria: Subjects meeting any of the following criteria must not be enrolled in the study: 1. Pregnant or lactating females; 2. Significant neurological or psychiatric disorders (psychotic disorders, dementia or seizures) that would prohibit the understanding and giving of informed consent; 3. History of serious cardiovascular/ cerebrovascular /hepatic /renal/hematopoietic diseases; 4. History of another malignancy; 5. Hypersensitivity to any drug of the study regimen; 6. Participated in other clinical trials within 3 months.

Design outcomes

Primary

MeasureTime frame
endoscopic;Biopsy histologic examination;Chest CT;

Countries

China

Contacts

Public ContactCai Yidong

China Academy of Chinese Medical Sciences Xiyuan Hospital

nmdrcyd@126.com+86 13910039501

Outcome results

None listed

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