Comparative study on the sedative effect of ketamine, magnesium sulfate and propofol in endoscopy

Phase 3

Recruiting

• Conditions: Condition 1: Diseases of upper digestive system which need endoscopy. Condition 2: Diseases of upper digestive system which need endoscopy.; Gastric ulcer; Barrett's esophagus; K22.7

• Registration Number: IRCT20161205031252N12
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 February 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 201

Inclusion Criteria

Patients aged more than 12 years

Exclusion Criteria

History of allergy to medications
ASA physical status classification system more than 3

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Physician's satisfaction of the adequacy of sedation for performing endoscopy. Timepoint: Immediately after completing the endoscopy. Method of measurement: Comfort score.;Patient's satisfaction of the adequacy of sedation for performing endoscopy. Timepoint: Immediately after completing the endoscopy. Method of measurement: Comfort score.;Sedation response score. Timepoint: Immediately after completing the endoscopy. Method of measurement: Ramsay sedation scale.

Secondary Outcome Measures

Name	Time	Method
Recovery time. Timepoint: At the time of leaving recovery. Method of measurement: Time recording.