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Clinical Trial Summary

To clarify the clinical effect of Ganoderma lucidum spore powder intervention on postoperative depressive symptoms of papillary thyroid carcinoma ; to elucidate the antidepressant mechanism of Ganoderma lucidum spore powder.


Clinical Trial Description

After being informed of the study and potential risks, all patients who gave written informed consent were enrolled. A total of 300 eligible patients were randomly assigned in a double-blind manner and divided into experimental group and control group at a ratio of 2 : 1. The subjects were given oral test drugs ( Ganoderma lucidum spore powder or placebo ) 4g per day for 90 days from the first day after enrollment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06429514
Study type Interventional
Source Zhejiang Cancer Hospital
Contact
Status Completed
Phase N/A
Start date March 28, 2023
Completion date May 3, 2024

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