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Sedation Of Adult Patients Undergoing Gastrointestinal Endoscopy: A Network Meta-analysis
Sedation Of Adult Patients Undergoing Gastrointestinal Endoscopy: A Network Meta-analysis
CompletedN/A
Sponsor: Pfizer
Conditions: Gastrointestinal Endoscopy, Sedation, Dexmedetomidine
Interventions: Dexmedetomidine, Midazolam, Propofol, Midazolam/Propofol
Countries: South Korea
The objective of this study is to compare the efficacy and safety of dexmedetomidine with other sedatives in sedation during endoscopy by analyzing the most recently published interventional trials and observational studies.
Eligibility overview
Sex: ALL
Age: 12 Years to —
Healthy volunteers: No
Study type: OBSERVATIONAL
Eligibility criteria
* Inclusion criteria We will include studies if they (1) the setting was using any sedative for endoscopy for an procedural sedation (2) the study compared dexmedetomidine with other sedative for sedative therapy and (3) the outcomes included satisfaction score and adverse events. * Exclusion criteria We excluded studies if they (1) the number of sedative was different in two arms (2) did not report the specific results comparing dexmedetomidine with other sedatives.
Locations (1)
- Seoul, South Korea