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Study on Objective Characterization and Application of Acupuncture Deqi Based on Multimodal Technology

Study on Objective Characterization and Application of Acupuncture Deqi Based on Multimodal Technology

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047517
Enrollment
Unknown
Registered
2021-06-20
Start date
2021-06-15
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Healthy Subject

Interventions

Sponsors

Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Gender is not limited, aged 18 to 40 years, in good health; 2. Body weight: 45 ~ 80kg, BMI: 19 ~ 24; 3. Regular daily life, no smoking, drinking, long-term drinking of tea or coffee and other bad habits; 4. The physical examination items were normal, no positive signs of clinical significance were found in physical examination, no history of organic diseases, no history of heart, liver, spleen, lung, kidney, digestive tract, nervous system, no chronic physical diseases, no history of long-term drug treatment, no blood system diseases such as platelet abnormality, hemophilia, coagulation dysfunction, etc; 5. There was no mental disorder or family history of mental illness; 6. Those who did not receive acupuncture or cupping treatment within 7 days before the experiment; 7. No medication was taken within 3 weeks before the trial; 8. The subjects signed the informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Metal implants (metal dentures, fracture fixation plates, etc.); 2. The contraindications of acupuncture and moxibustion were syncope or blood sickness; 3. Self rating Anxiety Scale (SAS) standard score >= 50, self rating Depression Scale (SDS) standard score >= 50 or mini mental state examination (MMSE) < 27; 4. There are trauma, skin lesions, etc. in the body, or there are skin infections and ulcers around the needful acupoints; 5. Those who have participated in or are participating in other clinical studies within the past week of the trial; 6. Women in menstruation, pregnancy and lactation.

Design outcomes

Primary

MeasureTime frame
Needle sensation score of subjects;Score of operator's feeling of tightness;Integral EMG;Needle traction;Displacement and deformation of the tissue;Elasticity of the tissue;Oxyhemoglobin concentration;Deoxyhemoglobin concentration;

Secondary

MeasureTime frame
Root mean square of the EMG;Constitution of traditional Chinese Medicine;

Countries

China

Contacts

Public ContactGuo Yi

Tianjin University of Traditional Chinese Medicine

guoyi_168@163.com+86 13920921016

Outcome results

None listed

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