Quality of recovery in abdominal hysterectomy. Other complications of anesthesia
Conditions
Interventions
Intervention 1: Intervention group: 40 patients receive intravenous Propofol with induction dose of 2 mg/kg and 100 mcg/kg/min as an infusion dose produced by darmanyab pharmaceutical factory. Interve
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
30 Years to 65 Years
Inclusion criteria
Inclusion criteria: 80 female patients 30 to 65 years old with 1 and 2 stages of health based on American Society of Anesthesiologists(ASA) who are candidates for abdominal hysterectomy
Exclusion criteria
Exclusion criteria: Body Mass Index more than 30 kg/m2 Difficult airway Psychotic disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of recovery. Timepoint: 24 hours before surgery-24 hours after surgery-48 hours after surgery. Method of measurement: Questionnaire of quality of recovery-15.;Post operative pain. Timepoint: 24 hours before surgery-24 hours after surgery-48 hours after surgery. Method of measurement: Questionnaire of quality of recovery-15.;Nausea and vomiting. Timepoint: 24 hours before surgery-24 hours after surgery-48 hours after surgery. Method of measurement: Questionnaire of quality of recovery-15. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyedeh Golnaz Ziaei
Babol University of Medical Sciences
Outcome results
None listed