Rate of Blind Spot in Gastroscopy
Conditions
Interventions
6 groups:EndoAngel
Sponsors
Renmin Hospital of Wuhan University
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1) Males or females aged at least 18 years; 2) Gastroscopy is needed to further clarify the characteristics of digestive tract diseases; 3) Painless, ordinary and ultra-fine gastroscopy patients; 4) Able to read, understand and sign informed consent; 5) The investigator believes that the subjects can understand the clinical research process, are willing and able to complete all the research procedures and follow-up visits, and cooperate with the research procedures.
Exclusion criteria
Exclusion criteria: 1) Patiens have participated in other clinical trials, signed informed consent forms and were followed up in other clinical trials; 2) Patiens have participated in the clinical trial of the drug and during the eluting period of the experimental drug or the control drug; 3) drug or alcohol abuse or mental disorder in the last 5 years; 4) pregnant or lactating women; 5) subjects with previous history of gastric surgery or diagnosed with gastric stump; 6) allergic to preused anesthetic drugs was found in previous medical history; 7) prior history of spasmolytic agent allergy; 8) the investigator considers that the subject is not suitable for painless or general or ultrafine gastroscopy; 9) the investigator considers that the subjects are not suitable for high-risk diseases or other special circumstances of the clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blind spot rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blind spot rate;Operation time;Comfort degree;Limb coordination;Vomiting reaction; | — |
Countries
China
Contacts
Public ContactYu Honggang
Department of Gastroenterology, Renmin Hospital of Wuhan university
Outcome results
None listed