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A Multimodal Ultrasonographic Study on the Therapeutic Effects and Vagal Nerve Features of Acupuncture Using the 'Wenyang Huazhuo' Method in Simple Obesity

A Multimodal Ultrasonographic Study on the Therapeutic Effects and Vagal Nerve Features of Acupuncture Using the 'Wenyang Huazhuo' Method in Simple Obesity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002214
Enrollment
Unknown
Registered
2025-11-17
Start date
2026-04-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

obesity

Interventions

Intervention Group:Acupoints used in the intervention group: Baihui (GV20) ,Shenting (GV24) , Yintang (EX-HN3) , Shuifen (CV9) ,Tianshu (ST25), bilateral ,Shuidao (ST28), bilateral ,Sanyinjiao (SP6)
Control Group:Acupuncture will be applied at the following acupoints: Quchi (LI11), Tianshu (ST25), Daheng (SP15), Fenglong (ST40), and Yinlingquan (SP9), all bilaterally.

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with simple obesity according to Western medicine diagnostic criteria. 2.Aged between 18 and 60 years, regardless of sex. 3.No other weight loss interventions undertaken within 2 months prior to participation in this study. 4.Able to communicate effectively, provide a complete description of their condition, sign the informed consent form, and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1.Patients with secondary obesity, such as that caused by hypothalamic syndrome, pituitary tumors, Cushing's syndrome, hypogonadism, or drug-induced obesity, as well as those diagnosed with metabolic syndrome. 2.Pregnant or lactating women. 3.Patients with severe primary diseases affecting the cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic systems, or those with psychiatric disorders. 4.Individuals unable to provide informed consent due to intellectual disability or behavioral disorders. 5.Patients with suspected or confirmed history of alcohol or drug abuse. 6.Other conditions deemed by the investigators to reduce the likelihood of enrollment or complicate participation, such as frequent changes in work environment that may increase the risk of loss to follow-up.

Design outcomes

Primary

MeasureTime frame
Body weight;Waist circumference;Body Mass Index;

Secondary

MeasureTime frame
Changes in subcutaneous adipose tissue (SAT);Lipid profile;Changes in vagus nerve function;Changes in visceral adipose tissue (VAT);

Countries

China

Contacts

Public ContactMengqian Yuan

Affiliated Hospital of Nanjing University of Chinese Medicine

515347441@qq.com15895977391

Outcome results

None listed

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