About this trial
The goal of this clinical trial is to compare time of sedation between two drugs administered to patients undergoing upper gastrointestinal endoscopy Primary outcome : Time of sedation : is the time to reach sedation score of 5 according to modified Ramsay sedation score starting from the time of injecting bolts dose of study drugs
Secondary outcome :
* Recovery time :is the time to reach score 2 of modified Ramsay sedation score starting from injecting bolus dose of study drugs . * Hemodynamics (MAP,HR) \& oxygen saturation * Drug side effects (nausea,vomitting,agitation) * Endoscopist satisfaction
Eligibility criteria
Qualifiers
Patient acceptance
Adults aged 21-60 years.
Both sexes
BMI<35 kg/m2
Disqualifiers
• Known allergy to any of the study drugs
Unstable Cardiovascular disease
Moderate to severe respiratory diseases
Trial design
Treatments tested in this trial
- Not listed