Status:
NOT_YET_RECRUITING
A Real-world Clinical Study on the Treatment of Menopausal Syndrome With Liuwei Dihuang Pills
Lead Sponsor:
China Academy of Chinese Medical Sciences
Collaborating Sponsors:
Lanxi Hospital of Traditional Chinese Medicine
First Affiliated Hospital of Harbin Medical University
Conditions:
Menopausal Syndrome
Eligibility:
FEMALE
45-55 years
Brief Summary
To evaluate the clinical efficacy of the real-world Liuwei Dihuang pills for the treatment of female menopausal syndromes, and to provide a basis for effective, safe and rational clinical use of the d...
Detailed Description
In this study, the patients were divided into exposed and non-exposed groups based on whether or not they were taking Liuwei Dihuang Pills. The patients in the non-exposed group were treated routinel...
Eligibility Criteria
Inclusion
- Age: 45-55 years old
- Patients with menopausal syndrome using Liuwei Dihuang Pills
- Kidney Yin Deficiency Syndrome
Exclusion
- Individuals allergic to any components of the drug or excipients;
- Individuals with other endocrine diseases;
- Individuals with organic lesions of the reproductive system;
- Individuals who have undergone bilateral oophorectomy, hysterectomy, or have ovarian dysfunction;
- Individuals with endometrial hyperplasia or unexplained vaginal bleeding;
- Individuals with malignant tumors, hematologic, or immune system diseases;
- Individuals with severe cardiovascular, cerebrovascular, liver, or kidney diseases (e.g., serum transaminase levels more than 1.5 times the upper limit of normal, serum creatinine above the upper limit of normal);
- Individuals with psychiatric disorders or dependence on alcohol or drugs;
- Individuals with mental illness or communication barriers;
- Individuals with other conditions that, in the investigator's judgment, may reduce the likelihood of enrollment or complicate the study process are not suitable for participation in this clinical research.
Key Trial Info
Start Date :
March 8 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 30 2026
Estimated Enrollment :
1000 Patients enrolled
Trial Details
Trial ID
NCT06874738
Start Date
March 8 2025
End Date
December 30 2026
Last Update
March 13 2025
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