High dose Xiang Ju Ru Pi Ning capsule
Drugxingjurupining capsule,8 capsule,tid,3 months.
Other names: High dose group
NCT Number: NCT04229706
The study is to evaluate the efficacy and safety of two doses of xiangjurupining capsule in Hyperplastic disease of breast patients .
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Notify Me18 year–50 year
Female
Interventional
Phase 2
Baoding No.1 Hospital of TCM, Baoding, China
The study is to evaluate the efficacy and safety of two doses of xiangjurupining capsule,give three times a day versus placebo in Hyperplastic disease of breast patients .The clinical phase of the study comprises a run-in period,an 3-months double-blind treatment period and a 1-month follow-up period, resulting in 5-months overall duration of the study for each patient.
Patients report their breast pain as measured using NRS scale on the subject daily diary。
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
xingjurupining capsule,8 capsule,tid,3 months.
Other names: High dose group
xiangjurupining capsule,4 capsules , and xiangjurupining capsule placebo,4 capsules,tid,3 months.
Other names: Low dose group
xiangjurupining capsule,8 capsule,tid,3 months.
Other names: Placebo group
Time frame: up to 3 months
Subject reported breast pain using NRS( Numerical Rating Scale)scale on the subject daily diary..The NRS scale is a line composed of 11 points, marked with a scale of 0 to 10. The subjects rated themselves according to the most painful degree every day. The higher the score, the higher the degree of pain.
Time frame: up to 3 months
Subject reported breast pain as measured using NRS scale on the subject daily diary.The number of the pain days was calculated and compared with the baseline which the number of pain days in the lead-in period.
Time frame: 3 months after treatment
Assess the scope ,the size and the hardness of the target lump by palpation.The doctor palpated the breast of the subjects and measured the size of the target lump with a ruler.Four quadrant method was used to record the number of the target lump's quadrants.Four level(0,2,4,6) to measure The scope,the size and the hardness of lump .the Score from 0(none) to 6(most severe).
Time frame: 3 months after treatment
Assess the breast glandular section thickness, breast duct width and nodules of the target lump area by B-ultrasound.
Time frame: 3 months after treatment
Compared wth baseline,the scores of changes of TCM syndrome Evaluation at each visit .This instrument consists of two primary symptoms: breast pain, breast mass ,and four secondary symptoms.Four levels to measure severity of primary symptoms(0、2、4、6)and secondary symptoms(0、1、2、3), respectively. Record the tongue and pulse conditions. The TCM syndrome effect calculated by nimodipine method. The final score has a range of 0 to 100. The effect of TCM syndrome from 0% (negative ) to 100% (disappear).
Tasly Pharmaceutical Group Co., Ltd
Industry
A Randomized, Double-blind, Placebo-controlled, Multicenter Phase II Clinical Study on the Efficacy and Safety of Xiangjurupining Capsule in the Treatment of Hyperplasia of Breast (Liver Stagnation and Phlegm Coagulation)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.