Chronic Gastritis
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time frame |
|---|---|
| Pain Threshold Character;Temperature Characteristics;Microcirculation Characteristics;Oxygen Saturation Characteristics; Resistance Characteristics;GSRS; | — |
Secondary
| Measure | Time frame |
|---|---|
| SDS;SAS;PSQI;PGIC;Traditional Chinese Medicine Constitution Scale; | — |
Countries
China
Contacts
Zhejiang Chinese Medical University