ITMCTR2100004907
Recruiting
Phase 4
An observation study on the long-term efficacy of Huisheng oral solution after radical operation of stage II to IIIb non-small cell lung cancer (NSCLC)
Sichuan Provincial People's Hospital0 sitesTBD
Conditionson-small cell lung cancer(NSCLC)
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- on-small cell lung cancer(NSCLC)
- Sponsor
- Sichuan Provincial People's Hospital
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. The patient's aged \>\=18 years, and the gender is not limited;
- •2\. Radical surgical treatment has been performed in the research center (Thoracic Surgery Department of Sichuan Provincial People's Hospital);
- •3\. On the 5 ± 3 days after the operation, pathological examination was diagnosed as non\-small cell lung cancer, and according to the 8th edition of the International Society for the Study of Lung Cancer (IASLC) lung cancer TNM staging was stage II to IIIb;
- •4\. The investigator assessed complete remission (CR) after the operation;
- •5\. No history of allergies to the ingredients of Huisheng Oral Liquid in the past;
- •6\. Performance Status: 0\-1 points;
- •7\. The life expectancy is at least 12 weeks;
- •8\. Laboratory examinations confirmed that the patient's blood routine and liver and kidney functions were normal within 7 days before the first medication;
- •9\. The patient must have the ability to understand and voluntarily sign an informed consent form.
Exclusion Criteria
- •1\. Merge other tumors;
- •2\. Those with a history of deep vein thrombosis, pulmonary embolism, stroke, acute myocardial infarction, atrial fibrillation, patent foramen ovale, etc.;
- •3\. Patients with bleeding tendency or coagulation disorders;
- •4\.6 Those who have suffered acute spinal cord injury, have undergone joint replacement surgery, and have multiple traumas to hip, pelvic or lower limb fractures within 4\.6 months;
- •5\. Suffer from uncontrollable neurological, mental illness or mental disorder, and poor compliance;
- •6\. Patients who participate in other clinical trials at the same time;
- •7\. Other situations that the researcher thinks are not suitable for inclusion in the group.
Outcomes
Primary Outcomes
Not specified
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