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Clinical research of acupuncture with branch-foundation acupoint combination on prevention and treatment of perimenopausal syndrome

Clinical research of acupuncture with branch-foundation acupoint combination on prevention and treatment of perimenopausal syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009814
Enrollment
Unknown
Registered
2016-11-10
Start date
2016-11-03
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

perimenopause syndrome

Interventions

intervention group:acupuncture with branch-foundation acupoint combination
control group:routine selection of acupoints

Sponsors

Hubei Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnosis standard for perimenopausal syndrome in Practical Obstetrics and Gynecology released by People's Medical Publishing House, 2013; 2. Aged 40 to 55 years old; 3. the modified Kupperman score>15; 4. willing to participate and signing the inform consent.

Exclusion criteria

Exclusion criteria: 1. prior hysterectomy and/or oophorectomy; 2. with malignant cancer or history of chemotherapy and/or irradiation; 3. unstable thyroid disease; 4. Taking hormone medicines or other drugs associated with the diseases like black cohosh, phytoestrogens, clonidine, veralipride, SSRIs etc during the 12 weeks before the study; 5. With ovarian cysts or uterine fibroids with a diameter greater than 4cm or agnogenic vaginal bleeding; 6. With mandatory indications of hormone therapy, such as menopause after surgery, active osteoporosis, etc; 7. With serious heart, lung, liver, kidney, and nerve, blood system diseases and diabetic neuropathy; 8. Coagulation defeats, or taking anticoagulant drugs, such as warfarin, heparin, etc; 9. Dermal diseases, such as eczema, psoriasis, etc; 10. With smoking or drinking or drug abuse problems; 11. With mental illness and cant take care of themselves; 12. Low compliance; 13. Participate in other clinical trials. Meeting any one of the above 13 will not be included in this study.

Design outcomes

Primary

MeasureTime frame
Modified Kupperman score: changes and change rate in modified Kupperman score compared with baseline;

Secondary

MeasureTime frame
An average of 24 hours of hot points: changes in an average of 24 hours of hot points compared with baseline;MENQOL score: changes in MENQOL score compared with baseline;Serum level of sex hormone: changes in FSH, LH, E2 in serum compared with baseline;

Countries

China

Contacts

Public ContactZhou Zhong-yu

Hubei Provincal Hospital of Traditional Chinese Medicine

463275008@qq.com+86 18672308659

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026