functional dyspepsia
Conditions
Interventions
The experimental group:Percutaneous electroacupuncture stimulation(ST36, PC6)
The control group:Percutaneous electroacupuncture stimulation(sham ST36, sham PC6)
Sponsors
The Second Affiliated Hospital of Anhui Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Meet the diagnostic criteria for functional dyspepsia Rome IV postprandial discomfort syndrome or epigastric pain syndrome; 2. Aged 18-65 years old, male or female; 3. Gastroscopy should be performed in a tertiary hospital within one year before the selection to exclude gastric cancer, ulcer, erosive gastritis or other gastric organic diseases; 4. Hepatobiliary and pancreatic diseases have been excluded by B-ultrasound examination in a top-three hospital within one year before the selection; 5. Willing to sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Those with a history of abdominal surgery; 2. Take PPI, prokinetic, anticholinergic or dopaminergic drugs 2 weeks before and during the experiment; 3. Those with a history of diabetes, thyroid disease, systemic sclerosis, systemic lupus erythematosus, etc.; 4. Pregnant women, lactating women or those planning to become pregnant; 5. Those who are allergic to skin preparations and familiar with acupoints and functions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptom scores;Peripheral blood cytokines;The number of eosinophils and mast cells in gastroduodenal mucosa; | — |
Secondary
| Measure | Time frame |
|---|---|
| Cognitive scale measurement; | — |
Countries
China
Contacts
Public ContactHu Xiangpeng
The Second Affiliated Hospital of Anhui Medical University
Outcome results
None listed