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Research and Development of Intelligent Key Technologies and Equipment for Deqi in Frequency-Conversion Moxibustion with Demonstration and Application

Research and Development of Intelligent Key Technologies and Equipment for Deqi in Frequency-Conversion Moxibustion with Demonstration and Application

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001951
Enrollment
Unknown
Registered
2025-10-15
Start date
2024-12-30
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

dysmenorrhea

Interventions

Variable frequency group:Frequency conversion technique for moxibustion
Control group 1:Non variable frequency parameter 1 manual moxibustion
Control group 2:Non variable frequency parameter 2 manual moxibustion

Sponsors

Jiangxi University of Chinese Medicine Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Primary dysmenorrhea: 1) Meets the diagnostic criteria for primary dysmenorrhea mentioned above; 2) Women aged 18-30 who have not given birth and have regular menstrual periods (28 ± 7 days); 3) Heat sensitive acupoints appeared in the area where the patient applied moxibustion; 4) Being able to correctly express the induction of qi in moxibustion; 5) Patients who are willing to accept the treatment plan of this project. Non characteristic lower back pain: 1) Meets the above non-specific diagnostic criteria for lower back pain; 2) The patient is aged between 18 and 70 years old; 3) The patient has thermal sensitive acupoints in the waist Yangguan acupoint area; 4) Being able to correctly express the induction of qi in moxibustion; 5) Patients who are willing to accept the treatment plan of this project.

Exclusion criteria

Exclusion criteria: Primary dysmenorrhea: 1) Patients with primary dysmenorrhea who have menstrual disorders and cannot predict the treatment time; 2) Pregnant or lactating women; 3) Patients with severe primary diseases such as cardiovascular and cerebrovascular diseases, liver and kidney diseases, lung diseases, and hematopoietic systems, as well as psychiatric patients; 4) According to researchers' judgment, other lesions or conditions that may reduce the likelihood of inclusion or complicate inclusion, such as frequent changes in work environment, unstable living environment, etc., can easily lead to loss to follow-up. Non specific back pain: 1) Individuals with clear pathological changes, such as infections, tumors, tuberculosis, deformities, lumbar disc herniation, nerve root syndrome or cauda equina syndrome, fractures, severe osteoporosis, etc; Individuals with obvious symptoms of spinal cord compression or nerve root injury; 2) Pregnant or lactating women; 3) Patients with severe primary diseases such as cardiovascular and cerebrovascular diseases, liver and kidney diseases, lung diseases, and hematopoietic systems, as well as psychiatric patients; 4) According to researchers' judgment, other lesions or conditions that may reduce the likelihood of inclusion or complicate inclusion, such as frequent changes in work environment, unstable living environment, etc., can easily lead to loss to follow-up.

Design outcomes

Primary

MeasureTime frame
Deqi intensity;

Secondary

MeasureTime frame
Deqi incubation period;Deqi accumulation time;Deqi dimension;

Countries

China

Contacts

Public ContactDingyi Xie

Jiangxi University of Chinese Medicine Affiliated Hospital

281999814@qq.com13970850489

Outcome results

None listed

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