PACTR201708002325400
Completed
未知
A randomized controlled trial comparing the proportion of hypoxia in sedated adults undergoing upper gastrointestinal endoscopy using target controlled infusion of propofol versus intermittent boluses.
The Aga Khan University, Nairobi0 sites176 target enrollmentMay 26, 2017
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Respiratory
- Sponsor
- The Aga Khan University, Nairobi
- Enrollment
- 176
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All ASA I and II adults aged 18 \- 65 years scheduled to undergo non\-emergent upper gastrointestinal endoscopy under sedation.
Exclusion Criteria
- •¿Known allergy to propofol, midazolam, soybean, egg.
- •¿Active respiratory tract infection.
- •¿History or indicator of large airway compromise e.g. obstructive sleep apnoea, COPD, presence of stridor, or known history of difficult bag\-valve\-mask ventilation.
- •¿Patients requiring additional types of sedative agents to achieve optimal sedation.
- •¿History of chronic exposure to sedative medication.
Outcomes
Primary Outcomes
Not specified
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