Comparison of dexmedetomidine with propofol in maintaining adequate depth of anesthesia

Phase 3

Recruiting

• Conditions: Anesthesia.; Anaesthetic, unspecified; Y48.4

• Registration Number: IRCT20151107024909N12
• Lead Sponsor: Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 November 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients over 20 years
Patients who are candidates for laparotomy surgery
Surgery with a time of more than 3 hours under general anesthesia

Exclusion Criteria

Patients over 60 years
Emergency surgery
Contraindications to the use of dexmedetomidine
Pregnancy or breastfeeding
Drug addiction
Uncontrolled blood pressure
Body mass index above 30

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depth of anesthesia. Timepoint: At the beginning and during surgery. Method of measurement: Anesthesia depth monitoring device.;Pain level of patients. Timepoint: From the beginning of recovery every 15 minutes up to three times. Method of measurement: Visual analog scale.;Agitation score. Timepoint: From the beginning of recovery every 15 minutes up to three times. Method of measurement: Based on the information in the patient's file.;Sedition score. Timepoint: From the beginning of recovery every 15 minutes up to three times. Method of measurement: Based on the information in the patient's file.