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Clinical Trial Summary

To observe the improvement of Chalder scale score in patients with chronic fatigue syndrome treated by compound Ciwujia granules. Improvement =[(baseline score - post-treatment score)/baseline score]*100%


Clinical Trial Description

After being informed of the study and potential risks, all subjects who have given informed consent undergo a 2-week screening period to determine eligibility, and on day 0, subjects who meet eligibility requirements will be randomly assigned in a double-blind way. The patients were treated with compound Xiwujia granules + Guipi granules/placebo (experimental group) and compound Xiwujia granules/placebo + Guipi granules (positive control group) at a ratio of 1:1 for 6 weeks. Compound Ciwujia granules/placebo 8g per bag, 2 times a day, 1 bag each time, Guipi granules, 3g per bag, taken with boiling water. 1 bag (3g) at a time, 3 times a day. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06245642
Study type Interventional
Source Heilongjiang Quanle Pharmaceutical Co., Ltd.
Contact Weian Yuan, Doctor
Phone 13774269261
Email weian_1980@163.com
Status Not yet recruiting
Phase Phase 4
Start date March 1, 2024
Completion date November 1, 2025

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