Spinal surgery. Fusion of spine, site unspecified
Conditions
Interventions
Intervention 1: Intervention group 1: Patients in this group will be infused with doxapram(BehbodDaroo Company) 1 mg / kg for three hours. Intervention 2: Intervention group 2: Patients in this group
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Age category 70-18 years Class I and II classification of the American Society of Anesthesiologists(ASA) Candidate for spine surgery Satisfaction to participate in the study
Exclusion criteria
Exclusion criteria: Existence of confirmed cerebral edema Sensitivity to the studied drugs Having hemoglobin less than 9 g/dL Having a history of underlying diseases (such as cardiovascular disease, lung disease, hypertension, hyperthyroidism)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Respiratory Rate. Timepoint: Half an hour before entering the intensive care unit and at 6, 12, 18, 24, 30, 36, 42, 48 hours after intervention. Method of measurement: Ventilator device.;Oxygen saturation(SPO2). Timepoint: Half an hour before entering the intensive care unit and at 6, 12, 18, 24, 30, 36, 42, 48 hours after intervention. Method of measurement: Ventilator device.;Blood pressure. Timepoint: Half an hour before entering the intensive care unit and at 6, 12, 18, 24, 30, 36, 42, 48 hours after intervention. Method of measurement: Ventilator device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBabak Alikiaii
Esfahan University of Medical Sciences
Outcome results
None listed