Sedation. Other and unspecified general anaesthetics
Conditions
Interventions
Intervention 1: The Intervention group receives 1 mg midazolam and0.5 mg/kg ketamine before ERCP and 0.5 mg / kg propofol as a rescue bolus dose then followed by 75microgram / kg / min infusion. Int
Treatment - Drugs
The Intervention group receives 1 mg midazolam and0.5 mg/kg ketamine before ERCP and 0.5 mg / kg propofol as a rescue bolus dose then followed by 75microgram / kg / min infusion
the control group receives midazolam 1 mg and fentanyl 50 to 100 micrograms before ERCP and 0.5 mg / kg propofol as a rescue bolus dose and then followed by 75microgram / kg / min infusion
Sponsors
Vice-chancellor of research of Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: age 18-80 years; ASA class = 3 Exclusion criteria: age 80 years; Heart disease (arrhythmias, Aortic Stenosis, Ischemic Heart Disease,Heart failure) ; liver disease (Child-Pugh classification C); drug addiction.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sedation. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: Ramsay Sedation Scale.;Pain. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: Visual Analoge Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: sphygmomanometer.;Respiratory Rate. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAmri Maleh Parviz
Vice-chancellor of research of Babol University of Medical Sciences
Outcome results
None listed