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Clinical Trial Summary

This study is designed as a multi-center, randomized, double-blind, placebo-controlled trial. Subjects in the intervention group will be treated with XLJDOD compound granule. Subjects in the control group will be treated with placebo (XLJDOD mimetic agent).


Clinical Trial Description

Subjects in the intervention group will be treated with XLJDOD compound granule. Treatment will begin within 3 months after standard adjuvant chemotherapy and compliance will be continuously monitored. XLJDOD will be taken twice a day, infused with warm water, 1 hour after lunch and dinner. One course of treatment will take 28 days in 1 month, and 2- to 3-day rest. Treatment will continue for 6 courses. Subjects in the control group will be treated with placebo (XLJDOD mimetic agent). The course of placebo in control group will be in accordance with that of XLJDOD in intervention group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05709249
Study type Interventional
Source Jiangsu Famous Medical Technology Co., Ltd.
Contact Yujia Wang
Phone 18120192802
Email 1217909635@qq.com
Status Recruiting
Phase Phase 3
Start date December 1, 2022
Completion date December 1, 2025

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