Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Cirrhosis, Liver
Type
Interventional
Phase
Phase 3
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Care Provider)Primary Purpose: Treatment

Participation Requirements

Age
Between 45 years and 65 years
Gender
Both males and females

Description

Effect of use of propofol versus use of midazolam as sedative agent in patients with liver cirrhosis presented for lower gastrointestinal endoscopy, Randomised controlled trial.

Effect of use of propofol versus use of midazolam as sedative agent in patients with liver cirrhosis presented for lower gastrointestinal endoscopy, Randomised controlled trial.

Tracking Information

NCT #
NCT03388151
Collaborators
Not Provided
Investigators
Principal Investigator: Sherief Abd-Elsalam, MD Gastroenterology Study Director: Sameh Abdelkhalek Ahmed, MD Tanta University Anasthesia Department