Comparison of the effect of two drugs on hemodynamic changes and sedation in recovery.
Conditions
Interventions
Intervention 1: Intervention group: Patients are divided into two groups. The first group: propofol from Tehran Shimi Pharmaceutical Company with a dose of 75-125 mcg/kg/hour until the end of the oper
It is injected until the end of the procedure.
Sponsors
Yasouj University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Candidate patients for elective laparoscopic cholecystectomy surgery under general anesthesia ASA class I No history of addiction No co-morbidities No use of benzodiazepines Consent to participate in the study Not being allergic to the study drugs Absence of pregnancy or breastfeeding
Exclusion criteria
Exclusion criteria: The need for simultaneous surgery Changing the surgical method to classic open cholecystectomy Recovery time more than forty-five minutes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systolic pressure changes. Timepoint: Every 10 minutes from the start of the operation to discharge from recovery. Method of measurement: Use of sphygmomanometer.;Investigation of agitation in recovery. Timepoint: Every 10 minutes from the start of the operation to discharge from recovery. Method of measurement: Richmond Agitation-Sedation Scale.;Diastolic pressure changes. Timepoint: Every 10 minutes from the start of the operation to discharge from recovery. Method of measurement: Use of sphygmomanometer.;Investigation of sedation in recovery. Timepoint: Every 10 minutes from the start of the operation to discharge from recovery. Method of measurement: Richmond Agitation-Sedation Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAfshin Mansourian
Yasouj University of Medical Sciences
Outcome results
None listed