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Clinical trial study on central response characteristics of acupuncture at the hand 12 Jing-Well points in healthy population

Clinical trial study on central response characteristics of acupuncture at the hand 12 Jing-Well points in healthy population

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052374
Enrollment
Unknown
Registered
2021-10-24
Start date
2021-11-16
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Healthy population

Interventions

Before and after control group:acupuncture at the hand 12 Jing-Well points

Sponsors

Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Gender is not limited, aged 20 to 50 years; 2. BMI between 18.5 and 23.9; 3. No smoking history, alcohol addiction history, no history of drinking strong tea and coffee; 4. The physical examination items are normal, no clinically significant positive signs are found in the physical examination, no history of organic diseases, no history of heart, liver, spleen, lung, kidney, digestive tract, nervous system, etc., no chronic physical diseases, no long-term drugs Treatment history, no blood system diseases such as platelet abnormalities, hemophilia, and coagulation disorders; 5. The individual has no mental disorder or family history of mental illness, and has no recent negative emotions such as depression and anxiety; 6. Not taking any drugs within three weeks before the test; 7. Right-handed; 8. There are no contraindications for clinical fMRI scanning (such as those with cardiac pacemakers; those with intracranial artery dissection; those with various metal implants in the body; those with critical illness, epilepsy, and claustrophobia; Tolerate fMRI examination for about 55 minutes); 9. After explaining the specific implementation steps of the test in detail to the subjects, the subjects voluntarily signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Women's pregnancy and menstrual period; 2. The body has trauma, skin lesions, etc., or there is skin infection or ulcer at the desired acupoint and its surroundings; 3. Participated in or participated in other clinical investigators during the trial within three months before the trial; 4. Those with a history of fainting needles and haemorrhages.

Design outcomes

Primary

MeasureTime frame
Central response characteristics of acupuncture at the hand 12 Jing-Well points in promoting wakefulness;

Countries

China

Contacts

Public ContactXu Zhifang

School of Acupuncture & Moxibustion and Tuina, Tianjin University of Traditional Chinese Medicine

xuzhifangmsn@hotmail.com+86 15822881626

Outcome results

None listed

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