Comparison of propofol sedation and lidocaine-propofol combination in patients undergoing bronochoscopy

Phase 3

Recruiting

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

• Registration Number: IRCT20160307026950N57
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

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

Inclusion Criteria

Minimum 18 years of age and maximum 60
ASA I or ASA II group of patients
Bronchoscopy candidate either male or female

Exclusion Criteria

Analgesics or Opioid use 24 hours before procedure
Previous use of Beta blockers
Any known allergy to drugs used in this trial
Patients with a past medical history of severe cardiovascular diseases, Asthma, Renal disease, Hepatic disease, chronic respiratory disease
Past history of Drug Allergy
Immunodeficiency
Alcohol consumption 24 hours before procedure
Muscular weakness

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Heart rate. Timepoint: Before induction, 3 minutes after induction, 10 minutes after induction, 20 minutes after induction. Method of measurement: ???? ????????.;Blood Pressure. Timepoint: Before induction, 3 minutes after induction, 10 minutes after induction, 20 minutes after induction. Method of measurement: non invasive manometer.

Secondary Outcome Measures

Name	Time	Method
Sedation level. Timepoint: Before induction, 3 minutes after induction, 10 minutes after induction, 20 minutes after induction. Method of measurement: Sedation Score.