Anaesthesia. Anaesthetic, unspecified
Conditions
Interventions
Intervention 1: Propofol
for each patient an stat dose of propofol 1 mg/kg is calculated and then injected. After the initial induction if sedation score 5 is not achieved, propofol infusion with the rate of 70 µg/kg/min will
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Sedation level. Timepoint: Before induction, 3 minutes after induction, 10 minutes after induction, 20 minutes after induction. Method of measurement: Sedation Score. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBehzad Nazemroaya
Esfahan University of Medical Sciences
Outcome results
None listed