Actively Recruiting
Efficacy of Dexmedetomidine-Propofol Versus Ketamine-Propofol for Sedation
Led by Sohag University · Updated on 2025-01-03
100
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to compare efficacy of sedation between Dexmedetomidine-Propofol and Ketamine-Propofol combinations in the upper or lower gastrointestinal system endoscopy. We compare between 2 combinations as regard hemodynamic stability, post operative side effects as occurrence of delirium, nausea, vomiting, headache, hallucination or agitation.
CONDITIONS
Official Title
Efficacy of Dexmedetomidine-Propofol Versus Ketamine-Propofol for Sedation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- American Society of Anesthesiologists physical status I to II
- Age between 18 and 60 years
- Both sexes
You will not qualify if you...
- Severe heart, lung, liver disease, kidney failure, or bleeding disorder
- Fever, hypothermia, infection, electrolyte disorders such as hypokalemia and hypocalcaemia, acid-base disorder
- Allergy to drugs to be used
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Sohag University Hospital
Sohag, Egypt
Actively Recruiting
Research Team
A
Ahmed H Hamed, Resident
CONTACT
A
Alhaddad A Mosa, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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