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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

NCT03632330

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