Clinical trial · Observational
Adverse Events During Upper Gastrointestinal Endoscopy
Adverse Events During Upper Gastrointestinal Endoscopy With and Without Sedation: a Multiple Center Report From Shanghai
NCT01979549CI-TRIAL-00013513AEDUGESSHunknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The primary objective is to investigate the adverse events during upper gastrointestinal endoscopy with and without sedation in Chinese population
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Esophagus Cancer | — | UNRESOLVED | — |
| Gastric Cancer | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
| Oesophagitis | — | UNRESOLVED | — |
| Patients Need Upper Gastrointestinal Endoscopy | — | UNRESOLVED | — |
| Peptic Ulcer | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (2)
- label
- Sedation
- description
- patients underwent upper gastrointestinal endoscopy with sedation
- label
- non-sedation
- description
- patients underwent upper gastrointestinal endoscopy without sedation
Primary outcomes (1)
- measure
- Adverse events
- timeFrame
- Patients will be followed for the duration of hospital stay, an expected average of 2 hours
- description
- Investigate the adverse events according to the Adverse event reporting tool of the world SIVA International Sedation Task Force during upper gastrointestinal endoscopy with and without sedation.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.