Patients Need Upper Gastrointestinal Endoscopy | Adverse Events During Upper Gastrointestinal Endoscopy
Patients Need Upper Gastrointestinal Endoscopy research study
What is the primary objective of this study?
The primary objective is to investigate the adverse events during upper gastrointestinal
endoscopy with and without sedation in Chinese population
Who is eligible to participate?
- Patients will undergo upper gastrointestinal endoscopy
- Age > 18 years old
- Signed informed consent form
- Allergy to propofol or soybean or albumen
Which medical condition, disease, disorder, syndrome, illness, or injury is researched?
Patients Need Upper Gastrointestinal Endoscopy
Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.
Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.
Sedationpatients underwent upper gastrointestinal endoscopy with sedation
non-sedationpatients underwent upper gastrointestinal endoscopy without sedation
Start Date: December 2013
Completed Date: December 2014
Primary Outcome: Adverse events
Study sponsors, principal investigator, and references
Principal Investigator: Diansan Su, Doctor
Lead Sponsor: RenJi Hospital
Collaborator: Shanghai Pudong New Area People's Hospital