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Not Yet RecruitingNCT06874738

A Real-world Clinical Study on the Treatment of Menopausal Syndrome With Liuwei Dihuang Pills

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
China Academy of Chinese Medical Sciences · Academic / Other
Sex
Female
Age
45 Years – 55 Years
Healthy volunteers
Not accepted

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 drug.

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 routinely, and the patients in the exposed group were treated routinely + Liuwei Dihuang Pills. The patients in the exposed group were required to take the medication according to the dosage instructions for at least 4 consecutive weeks. Combined use of drugs is allowed without interfering with the treatment plan, and the use of drugs and combined use of drugs should be recorded truthfully, including the dose, duration, frequency, and so on. The type of drugs used in combination and the corresponding daily dose, daily frequency and duration of treatment. During the course of treatment, patients in both groups were required to receive follow-up assessment once every 4 weeks. Termination of the study included death, loss of patients, or achievement of study endpoints.

Conditions

Interventions

TypeNameDescription
DRUGLiuwei Dihuang pillsConventional treatment (Hormones, selective 5-hydroxytryptamine reuptake inhibitors, etc.)+ Liu Wei Di Huang Pills

Timeline

Start date
2025-03-08
Primary completion
2026-12-30
Completion
2026-12-30
First posted
2025-03-13
Last updated
2025-03-13

Source: ClinicalTrials.gov record NCT06874738. Inclusion in this directory is not an endorsement.