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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?

Inclusion Criteria: - Patients will undergo upper gastrointestinal endoscopy - Age > 18 years old - Signed informed consent form Exclusion Criteria: - Pregnant - Allergy to propofol or soybean or albumen

Which medical condition, disease, disorder, syndrome, illness, or injury is researched?

Patients Need Upper Gastrointestinal Endoscopy

Peptic Ulcer

Gastric Cancer

Esophagus Cancer

Oesophagitis

Study Interventions

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.

Study Arms

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

Study Status

Unknown status

Start Date: December 2013

Completed Date: December 2014

Phase:

Type: Observational

Design:

Primary Outcome: Adverse events

Secondary Outcome:

Study sponsors, principal investigator, and references

Principal Investigator: Diansan Su, Doctor

Lead Sponsor: RenJi Hospital

Collaborator: Shanghai Pudong New Area People's Hospital

More information:https://clinicaltrials.gov/show/NCT01979549

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