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Recruiting NCT06756594
Efficacy of Dexmedetomidine-Propofol Versus Ketamine-Propofol for Sedation
Trial Parameters
Condition Propofol
Sponsor Sohag University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 100
Sex ALL
Min Age 18 Years
Max Age 60 Years
Start Date 2024-11-12
Completion 2025-06-11
Interventions
Dexmedetomidine-PropofolKetamine-Propofol
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * American Society of Anesthesiologists physical status I to II. * Age between 18 and 60 years. * Both sexes. Exclusion Criteria: * Having severe heart, lung, liver disease, kidney failure, or bleeding disorder. * Patients having fever, hypothermia or infection, electrolyte disorders, such as hypokalemia and hypocalcaemia, acid-base disorder, allergy to drugs to be used.