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Efficacy and Safety of Traditional Chinese Medicine Intervention for Women With Menopausal Syndrome

Efficacy and Safety of Combined Treatment of Herbs and TCM Emotion Treatment for Women With Menopausal Syndrome: A Multiple-centered Randomized Controlled Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00933725
Enrollment
194
Registered
2009-07-07
Start date
2009-08-31
Completion date
2011-06-30
Last updated
2012-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menopausal Syndrome

Keywords

menopausal syndrome, TCM intervention

Brief summary

The purpose of this multiple-centered, randomized, controlled study is to investigate the efficacy and safety of a combination using herbs prescription and traditional Chinese medicine (TCM) emotion treatment in women with menopausal syndrome.

Detailed description

Menopausal syndrome is a high incident disease which is associated with great influence in women's health and quality of life. It involves physical discomforts and emotional symptoms. Traditional Chinese medicine (TCM) theory emphasizes treating physical and emotional symptoms simultaneously viewing one person as an entirety. Herbs prescription and TCM emotion treatment is effective and safe to treat women with menopausal syndrome in clinical practice.

Interventions

Drug: Particle of compound Chinese herbs(produced by San\_jiu Medical & Pharmaceutical Limited Company, Guangzhou, Guangdong Province, China), mixing with boiled water, free of decoction, taken orally, twice a day, for two months. One tablet placebo of Tibolone (provided by San\_jiu Medical & Pharmaceutical Limited Company, Guangzhou, Guangdong Province, China, once every two days, taken orally, for two months. Behavioral: TCM emotion treatment: made under the guide of TCM theory, administered by qualified TCM physician, for three times in two months.

OTHERWestern intervention

Drug: Tibolone, (produced by Oujianong corporation, Nanjing, China), 2.5mg, once every two days, taken orally, for two months; Particle placebo of compound Chinese herbs (produced by San\_jiu Medical & Pharmaceutical Limited Company, Guangzhou, Guangdong Province, China), mixing with boiled water, free of decoction, taken orally, twice a day, for two months. Behavioral: supportive psychotherapy, administered by qualified physician, for three times in two months.

Sponsors

Guangzhou University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
41 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Aged 41-60; * Amenorrhea for at least 6 months; * Menstruation dysfunction or cessation because of age or bilateral ovariectomy; * Hot flushes and night sweats symptoms; * Vaginal secretion decreased with or without dyspareunia; * Kupperman Index (KI) score ≥ 15; * Self-rating Anxiety Scale or Self-rating Depression Scale standard score \>50,but \<72(standard score= scale score ×1.25); * FSH ≥ 20 IU/L; * Thickness of endometrium ≤0.5cm if Amenorrhea for at least 12 months;or ≤1.5cm if Amenorrhea for 6 months to 12 months; * Meet the diagnosis criteria of TCM syndrome of liver stagnation and kidney deficiency.

Exclusion criteria

* With malignant tumor in reproductive system; * With benign tumor in reproductive system and need surgery; * Malignant tumor in mammary gland; * Irregular vaginal bleeding for unknown reasons; * Thickness of endometrium ≥1.5cm by ultrasound examination; * Have used Sex hormone medicine or joined other clinical trials 3 months before; * Allergy; * Severe diseases (eg., of the cardiovascular, liver, kidney) or uncontrolled endocrine diseases (eg., diabetes mellitus, hyperthyreosis ) * Severe psychiatric disease diagnosed by psychiatric physician; * Refuse informed consent.

Design outcomes

Primary

MeasureTime frame
Kupperman index2 months

Secondary

MeasureTime frame
blood serum estradiol2 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026