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Clinical study of heat-sensitive moxibustion for the treatment of somatic joint pain in menopausal syndrome

Clinical study of heat-sensitive moxibustion for the treatment of somatic joint pain in menopausal syndrome

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084687
Enrollment
Unknown
Registered
2024-05-22
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Menopausal syndrome

Interventions

Heat-sensitive moxibustion intervention group:Heat-sensitive moxibustion treatment for 15 days, once a day
Conventional massage control group:Conventional massage treatment for 15 days, once a day

Sponsors

Ganzhou Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Those who signed the informed consent form; (2) Those aged 40-60 years; (3) Those who are not menopausal; (4) Menopausal kupperman score =15; (5) Those who meet the diagnostic criteria of Chinese and Western medicine or have been clearly diagnosed by specialists; (6) Those with heat-sensitive moxibustion sensation.

Exclusion criteria

Exclusion criteria: (1) Serious cardiac and cerebrovascular diseases, psychiatric patients, and those who affect clinical observation; (2) Those who have undergone major gynaecological operations such as gynaecological tumours, hysterectomy, ovariectomy, etc. (3) Those who have taken sex hormone therapy in recent months. (4) Those who have stopped menstruation for more than 6 months. (5) Those who have gone through menopause.

Design outcomes

Primary

MeasureTime frame
Total Effective Rate;

Secondary

MeasureTime frame
Visual Analogue Score;Modified Kupperman Index;Menopause Rating Scale;

Countries

China

Contacts

Public ContactWang Qiang

Ganzhou Hospital of Traditional Chinese Medicine

846560448@qq.com+86 188 7072 5927

Outcome results

None listed

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