comparison of different doses of remifentanyl with the combination of propofol and meperidine on endotracheal intubation without muscle relaxant

Not Applicable

• Conditions: Opioids and related analgesics; endotracheal intubation.

• Registration Number: IRCT201310234923N4
• Lead Sponsor: Vice-chancellor Of Research Babol University Of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

inclusion criteria : patients aged between 18-35 , ASA? class I and II , general anesthesia ,undergoing orthopedic surgery

exclusion criteria : The patients with hypertention, cardiovascular problems, irritable air way, drug abuse, BMI above 30, addiction and possibility of difficult airway

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Endotracheal intubation. Timepoint: 60 seconds after drug injection. Method of measurement: evaluation of jaw relaxation ; laryngoscopy status ,vocal cord ,and coughing.

Secondary Outcome Measures

Name	Time	Method
Blood pressure. Timepoint: before intubation, after drug injection, in one, three and five minutes after endotracheal intubation. Method of measurement: cuff manometer.;Heart rate. Timepoint: before intubation, after drug injection, in one, three and five minutes after endotracheal intubation. Method of measurement: , puls oximetry.