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Clinical Trials/ITMCTR2100004896
ITMCTR2100004896
Recruiting
Phase 1

A randomized, double-blind, placebo-controlled trial of Qidong Bufei Decoction in treating postoperative symptoms of non-small cell lung cancer

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
non-small cell lung cancer
Sponsor
Guang'anmen Hospital, China Academy of Chinese Medical Sciences.
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Postoperative patients with stage I non\-small cell lung cancer diagnosed by pathology or cytology;
  • 2\. Enroll in the group within two weeks after thoracoscopy;
  • 3\. Aged 18\-75 years;
  • 4\. Physical condition score ECOG 0\-2 points;
  • 5\. Estimated survival period \>\= 6 months;
  • 6\. Neutrophils\>1\.5x10^9/L, platelets \> 100x10^9/L, hemoglobin\>9\.0g/dl; normal bilirubin or \< 1\.5xULN; AST (SGOT), ALT (SGPT)\< 2\.5xULN; serum creatinine \< 1\.5xULN.

Exclusion Criteria

  • 1\. Patients who received neoadjuvant chemotherapy before surgery;
  • 2\. Those who intend to receive radiotherapy, chemotherapy, targeted drug therapy and other treatment methods within 1 month after surgery;
  • 3\. Patients with severe complications such as pulmonary embolism, respiratory failure, and myocardial infarction during the perioperative period;
  • 4\. In other clinical trials;
  • 5\. Patients during pregnancy or lactation;
  • 6\. Patients with a history of mental illness that is difficult to control;
  • 7\. Those who are allergic to study drugs;
  • 8\. Those who cannot understand and refuse to sign the informed consent form;
  • 9\. Those who cannot cooperate with the scale data collector.

Outcomes

Primary Outcomes

Not specified

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