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Biological Characteristics-Based Study on the Correlation between Surface Body Signs and Internal Organs in Chronic Gastritis and the Efficacy Evaluation of Acupoint Needle-Embedding Therapy

Biological Characteristics-Based Study on the Correlation between Surface Body Signs and Internal Organs in Chronic Gastritis and the Efficacy Evaluation of Acupoint Needle-Embedding Therapy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081197
Enrollment
Unknown
Registered
2024-02-26
Start date
2024-02-26
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Chronic Gastritis

Interventions

Needle Embedding Therapy Group:Needle Embedding Therapy
Sham Needle Embedding Therapy Group:Sham Needle Embedding Therapy
Chronic Gastritis Observation Group:None

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for Healthy Volunteers: 1 Age = 18 and = 75 years, gender unrestricted; 2 Currently not experiencing symptoms of gastric discomfort such as epigastric fullness or pain, noisy acid reflux, or belching; 3 Past medical examinations confirm the absence of malignant tumors and severe underlying diseases in digestive, circulatory, respiratory, urinary, reproductive, endocrine, nervous systems, etc.; 4 Individuals who are conscious and capable of normal communication; 5 Individuals who understand and are willing to comply with the research protocol, and who have signed an informed consent form. Inclusion Criteria for Patients with Chronic Gastritis: 1 Conforms to the diagnostic criteria for chronic gastritis; 2 Patients confirmed to be without malignant tumors and severe underlying diseases; 3 Age = 18 and = 75 years, gender unrestricted; 4 Patients currently experiencing symptoms of gastric discomfort; 5 Patients who are conscious and capable of normal communication; 6 Patients who understand and are willing to comply with the research protocol, and who have signed an informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion Criteria for Patients with Chronic Gastritis: Patients with chronic gastritis who meet any of the following criteria will be excluded: 1. History of alcohol dependence or drug abuse, psychiatric disorders, and cognitive impairments that prevent cooperation with examinations and understanding of the study; 2. Female subjects who are pregnant or breastfeeding; 3. Patients with current abnormal body temperature; 4. Patients with concomitant gastric ulcers, functional dyspepsia, or other gastric diseases; 5. Subjects currently participating in other clinical trials. Exclusion Criteria for Healthy Volunteers. Healthy volunteers who meet any of the following criteria will be excluded: 1. History of alcohol dependence or drug abuse, psychiatric disorders, and cognitive impairments that prevent cooperation with examinations and understanding of the study; 2. Female subjects who are pregnant or breastfeeding; 3. Patients with current abnormal body temperature; 4. Subjects currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Pain Threshold Character;Temperature Characteristics;Microcirculation Characteristics;Oxygen Saturation Characteristics; Resistance Characteristics;GSRS;

Secondary

MeasureTime frame
SDS;SAS;PSQI;PGIC;Traditional Chinese Medicine Constitution Scale;

Countries

China

Contacts

Public ContactXiaomei Shao

Zhejiang Chinese Medical University

13185097375@163.com+86 189 5713 0287

Outcome results

None listed

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