Sedation. Failed moderate sedation during procedure
Conditions
Interventions
Intervention 1: Control group: : Fentanyl at a dose of one microgram per kilogram of body weight up to a maximum of 100 micrograms with first receiving 1 mg per kilogram of body weight of propofol as
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age18-65 years old Absence of cardiovascular disease ERCP candidate patients Do not take sedatives Absence of blood pressure Absence of respiratory disease Body Mass Index<30
Exclusion criteria
Exclusion criteria: History of drug abuse Medical allergy Kidney disease Liver disease Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Heart Rate. Timepoint: Before starting the procedure, 5 minutes after starting, 15 minutes after starting the procedure and after finishing the work. Method of measurement: Number per minute.;O2 saturation. Timepoint: Before starting the procedure, 5 minutes after starting, 15 minutes after starting the procedure and after finishing the work. Method of measurement: Pulse oximeter.;Sedation. Timepoint: Before starting the procedure, 5 minutes after starting, 15 minutes after starting the procedure and after finishing the work. Method of measurement: Ramsay score. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyed Hossein Hamidi
Babol University of Medical Sciences
Outcome results
None listed