- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06074809
RCT on the Treatment of Menopausal Syndrome With Chinese Medicine
Clinical Trial on the Treatment of Menopausal Syndrome With Chinese Medicine Gui-zhi-fu-ling-wan With Variation and the Mechanism of Anti-inflammation and Body Surface Temperature Distribution
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Menopausal syndrome is a series of symptoms caused by ovarian follicles degeneration that occurs before or after menopause. These symptoms include central nervous system-related disorders (such as hot flashes, insomnia, depression, anxiety, etc.); metabolic, weight, cardiovascular and musculoskeletal changes; urogenital and skin atrophy; and sexual dysfunction.
Some previous studies have investigated the possibilities of using traditional Chinese medicine (TCM) for the treatment of menopausal syndrome. However, due to the limitations of previous clinical research, more evidence is required to support the efficacy of TCM treatment. Therefore, we propose to conduct a randomized, double-blinded, placebo-controlled clinical trial here, with the hope of objectively assessing the efficacy and safety of using TCM to treat menopausal syndrome.
Study Type
Enrollment (Estimated)
Phase
- Phase 2
Contacts and Locations
Study Contact
- Name: Cho Wing Lo
- Phone Number: 35053476
- Email: louislo@cuhk.edu.hk
Study Contact Backup
- Name: Hongwei Zhang, PhD
- Phone Number: 39439845
- Email: zhanghw@cuhk.edu.hk
Study Locations
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-
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Shatin, Hong Kong
- School of Chinese Medicine
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female subjects with age between 40 and 60 years old;
- For those who have symptoms of primary menopause (irregular menstruation lasting for more than 6 months, or absence of menstrual periods for more than 3 months)
- The score of the physical symptoms in Greene Climacteric Symptom Score (GCS) is 6 or above (average level);
- Have moderate level (affecting certain level of daily activity) or severe (cannot carry out daily activity) hot flashes, defined as transient sensations of heat, sweating, flushing, anxiety and chills lasting for 1-5 minutes;
- Diagnosed Deficiency of Kidney essence and static blood in Lower Jiao by Chinese medicine practitioner
- Agreed to receive Chinese medication or placebo for 2 months upon randomization.
Exclusion Criteria:
- The menopausal syndrome caused by surgical operations or medications (such as chemotherapy, gonadotropin-releasing hormone agonists, etc.).
- Have received estrogen treatment in the past 2 months;
- Have received any medication for treating menopause in the past month, including herbs, non-prescribed drugs, supplements, or change of diet to consume more legumes;
- Known serious emotional, mental or psychological disorders that may affect the study;
- During pregnancy, pre-pregnancy period, or lactation period;
- Known history of allergy to any traditional Chinese medicine;
- Have received anticoagulant or antiplatelet drugs in the past month;
- Known history of some certain serious medical disease, such as cardiovascular disease, liver or renal dysfunction, diabetes, cerebrovascular disease, blood disorders, with unstable conditions;
- Chinese medicine pattern combined with damp phlegm or damp heat, or only deficiency of Yin blood or absence of static blood pattern.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Traditional Chinese medicine treatment group
Chinese medicine will be administered to patients in this group.
|
Modified Guizhi Fuling granules will be orally administered to patients in the TCM treatment group twice a day throughout the treatment period, which lasts for 8 weeks.
Other Names:
|
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Placebo Comparator: Placebo group
Placebo will be administered to patients in this group.
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Placebo will be orally administered to patients in the placebo group twice a day throughout the treatment period, which lasts for 8 weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Greene Climacteric Scale (Chinese version)
Time Frame: Week 8
|
Greene Climacteric Scale (GCS) is one of the most common scales used to assess menopause.
It includes four aspects of symptoms: vasomotor, somatic, psychological, and sexual response.
This scale consists of 21 symptoms that can be assessed by patients themselves.
The scoring from 0 to 3 in each item, indicates 'Not at all', 'A little bit', 'Much', and 'Very much' respectively.
|
Week 8
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Short-Form Health Survey, SF-12v2 (Chinese version)
Time Frame: Week 8
|
The SF-12v2 is the brief version of SF-36, consisting of 12 questions related to our physical, mental health and functionality.
It is used as a supportive tool to comprehensively assess the health status of the patient.
Scores range from 0 to 100, with higher scores representing better self-reported health.
|
Week 8
|
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Short-Form Health Survey, SF-12v2 (Chinese version)
Time Frame: Week 12
|
The SF-12v2 is the brief version of SF-36, consisting of 12 questions related to our physical, mental health and functionality.
It is used as a supportive tool to comprehensively assess the health status of the patient.
Scores range from 0 to 100, with higher scores representing better self-reported health.
|
Week 12
|
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Temperature change of face, limbs and abdomen
Time Frame: Week 8
|
The peripheral temperature of the face, limbs and abdomen of the patients will be measured by a thermographic camera.
|
Week 8
|
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Temperature change of face, limbs and abdomen
Time Frame: Week 12
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The peripheral temperature of the face, limbs and abdomen of the patients will be measured by a thermographic camera.
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Week 12
|
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Level change of sex hormones
Time Frame: Week 8
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Level change of Estradiol (E2) and Follicle-stimulating hormone (FSH) will be measured between baseline and week 8.
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Week 8
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Level change of sex hormones
Time Frame: Week 12
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Level change of Estradiol (E2) and Follicle-stimulating hormone (FSH) will be measured between baseline and week 12.
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Week 12
|
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Level change of inflammatory markers
Time Frame: Week 8
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Level change of the serum inflammatory factors: high-sensitivity C-reactive protein (hsCRP), Interleukin 6 (IL-6) , Interleukin 8 (IL-8) and Tumor necrosis factor-α (TNF-α) will be measured from baseline to week 8.
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Week 8
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Level change of inflammatory markers
Time Frame: Week 12
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Level change of the serum inflammatory factors: high-sensitivity C-reactive protein (hsCRP), Interleukin 6 (IL-6) , Interleukin 8 (IL-8) and Tumor necrosis factor-α (TNF-α) will be measured from baseline to week 12.
|
Week 12
|
|
Greene Climacteric Scale (Chinese version)
Time Frame: Week 12
|
Greene Climacteric Scale (GCS) is one of the most common scales used to assess menopause.
It includes four aspects of symptoms: vasomotor, somatic, psychological, and sexual response.
This scale consists of 21 symptoms that can be assessed by patients themselves.
The scoring from 0 to 3 in each item, indicates 'Not at all', 'A little bit', 'Much', and 'Very much' respectively.
|
Week 12
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hongwei Zhang, PhD, School of Chinese Medicine
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Menopause study
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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