laminectomy. vertebral column
Conditions
Interventions
Intervention 1: Intervention group 1: in propofol group 2-3 Mg/Kg propofol , o2 50%, N2o 50% was given. Intervention 2: Intervention group 2: in sevoflurane group 2-3 % Sevoflurane, o2 50%, N2o 50% w
Treatment - Drugs
Intervention group 1: in propofol group 2-3 Mg/Kg propofol , o2 50%, N2o 50% was given.
Intervention group 2: in sevoflurane group 2-3 % Sevoflurane, o2 50%, N2o 50% was given
Intervention group 3: in sevoflurane plus propofol group 2-3 % Sevoflurane and 2-3 Mg/Kg propofol was given.
Sponsors
Vice chancellor for research Ilam University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: patients candidate for laminectomy; age 20-70; same surgeon and anesthesia. Exclusion criteria: systemic disease
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 1,4,8,12,24 h after intervention. Method of measurement: Visual Analogue Scale (VAS).;Bleeding. Timepoint: During intervenation in surgery time. Method of measurement: pad.;Nausea & Vomiting. Timepoint: After intervention in recovery. Method of measurement: checklist and VAS.;Blood pressure. Timepoint: During intervenation in surgery time. Method of measurement: sphygmomanometer.;Hart rate. Timepoint: During intervenation in surgery time. Method of measurement: Pulse oximeter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Drug consumption. Timepoint: during 24 h after surgery. Method of measurement: Mg.;The first movement time. Timepoint: after intervention during discharge. Method of measurement: hrs.;Duration of recovery room. Timepoint: After intervention. Method of measurement: hrs.;Urinary retention. Timepoint: After intervention. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Khani
Ilam University of Medical Sciences
Outcome results
None listed