The comparison of two drug regimen: Isofluran-Remifentanil and Propofol -Remifentanil in blood pressure control and surgeon satisfaction in rhinoplasty surgery

Phase 2

Recruiting

• Conditions: Rhinoplasty surgery.; Encounter for cosmetic surgery; Z41.1

• Registration Number: IRCT20141009019470N95
• Lead Sponsor: Shiraz 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: 100

Inclusion Criteria

Patients Candidate for Rhinoplasty Surgery
Age 18-50 years
(ASA) I, II

Exclusion Criteria

Allergy to propofol and isoflurane or remifentanil
Hypertension
Cardiac Disease
Anemia
Liver Disease
Kidney Disease
CNS Disease
Previous Septo-rhinoplasty
COPD Disease
Sever Asthma

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Blood Pressure. Timepoint: Every 5 minutes in the operating room until the end of surgery and every 15 minutes in the recovery room until discharge. Method of measurement: Monitoring.;Surgeon satisfaction. Timepoint: End of surgery. Method of measurement: Likert scale.

Secondary Outcome Measures

Name	Time	Method
Heart Rate. Timepoint: Continuously during surgery until the end of recovery. Method of measurement: Monitoring.;Arterial Oxygen Saturation Percentage. Timepoint: Continuously during surgery until the end of recovery. Method of measurement: Pulse-oximeter.