Overview

Dexmedetomidine-ketamine Versus Propofol-ketamine for Sedation During Endoscopy in Hepatic Patients

Status:
Active, not recruiting
Trial end date:
2021-07-30
Target enrollment:
0
Participant gender:
All
Summary
We aim to compare the response to ketamine/dexmedetomidine and ketamine/propofol combinations used in hepatic patients with child-Pugh classification (class A), and early (class B) undergoing UGIE.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tamer Nabil Abdelrahman
Treatments:
Dexmedetomidine
Ketamine
Propofol
Criteria
Inclusion Criteria:

- hepatic patients with child-Pugh classification (class A), and (class B)

- American Society of Anesthesiologists physical status II, III

- aged 18 to 60 years

- scheduled for elective Upper gastro-intestinal endoscopy.

Exclusion Criteria:

- emergency gastro-intestinal endoscopy.

- patients with severe hepatic disorder (Child C) ,

- chronic neuro-psychiatric disorder,

- history of neuro-psychiatric drug intake,

- severe cardiovascular diseases,

- pregnancy,

- history of drug abuse, and

- history of allergy to any of the used drugs in the study