Chronic Gastritis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion Criteria for Chronic Gastritis Patients: ?Meet the diagnostic criteria for chronic gastritis; ?between 18 and 75 years, regardless of gender; ?No use of gastric protectants, antibiotics, gastrokinetic drugs, or other drugs that may affect clinical research within the last 4 weeks; ?Clear consciousness and ability to communicate normally; Understanding and willingness to comply with the research protocol and signing an informed consent form. Inclusion Criteria for Healthy Volunteers: ?Recent health examination report provided and cleared of any serious cardiac, pulmonary, digestive, urological, hematological, endocrine, or neurological diseases through physical examination by the researcher; ?No symptoms of postprandial upper abdominal fullness, pain, noisy reflux, or belching within the last week; ?Age between 18 and 75 years, regardless of gender; ?No use of drugs affecting clinical research within the last 4 weeks; ?Clear consciousness and ability to communicate normally; Understanding and willingness to comply with the research plan and signing an informed consent form.
Exclusion criteria
Exclusion criteria: Exclusion Criteria for Chronic Gastritis Patients: Chronic gastritis patients will be excluded if they meet any of the following criteria: ?Confirmed digestive system malignancies or other diseases by gastroscopy and pathology, or unclear etiology; ?Pregnant or lactating women; ?Individuals with mental disorders, alcohol dependency, drug abuse history, or cognitive impairments that prevent cooperation in examinations or understanding of the study; ?Severe primary diseases of the cardiovascular system, hematopoietic system, endocrine system, or conditions like systemic failure, diabetes, cancer, and Bleeding Tendency; ?Patients with abnormal body temperatures; ?Currently participating in other clinical trials. Exclusion Criteria for Healthy Volunteers: Chronic gastritis patients will be excluded if they meet any of the following criteria: ?Individuals with mental illness, severe depression, alcohol dependency, or a history of drug abuse; ?Pregnant or lactating participants; ?Volunteers with abnormal body temperatures; ?Currently participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Sensitivity Characteristics;Thermal Radiation Characteristics; | — |
Countries
China
Contacts
Zhejiang Chinese Medical University