Upper gastrointestinal disease
Conditions
Interventions
Observation Group:None
Sponsors
The Second Affiliated Hospital of Guangxi Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Aged 18-75 years, gender unlimited; 2.Electronic gastroscopy under anesthesia or sedation; 3.Voluntary participation in this clinical trial with written informed consent.
Exclusion criteria
Exclusion criteria: 1.Patients with contraindications to gastroscopy: (1)Patients with Thoracic and Abdominal Aortic Aneurysm; (2)Patients with high column deformity; (3)Patients with severe cardiac cerebrovascular disease; (4)Patients with severe cardiopulmonary insufficiency who could not tolerate gastroscopy; (5)Large diverticula in the upper digestive tract; (6)Acute inflammation of the upper digestive tract; (7)Patients with systemic bleeding disease or abnormal coagulation function and bleeding tendency; (8)Patients with mental disease or severe mental disorder and unable to cooperate with endoscopy; 2.Pregnant and lactating women; 3.Emergency gastroscopy and (or) treatment; 4.Previous history of upper gastrointestinal surgery; 5.Previous participation in other clinical trials 1 month prior to screening; 6.Previous history of allergy to narcotic drugs; 7.The researcher did not think it was suitable for the participants.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Image Quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of clinical experience;Instrument failure/defect rate; | — |
Countries
China
Contacts
Public ContactHuang Jiean
The Second Affiliated Hospital of Guangxi Medical University
Outcome results
None listed