Condition 1: sedation. Condition 2: analgesia.
Conditions
Interventions
Intervention 1: Intervention group 1: Initially, personal consent is obtained from the patients. Then the patient is placed on the operating bed and attached standard monitoring devices including puls
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 70 Years
Inclusion criteria
Inclusion criteria: The patients at the age of 15-70 years old ASAIII With breast cancer ASA I,II candidates for lumpectomy
Exclusion criteria
Exclusion criteria: Difficult airway management mental disorder allergy to drugs head Injury Severe cardiovascular disease Severe pulmonary disease history of Epilepsy or Seizure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean arterial pressure. Timepoint: Before and after the intervention, one, three, five, ten minutes after induction of anesthesia and then at 60 and 120 minutes. Method of measurement: Non invasive blood pressure Automated.;Heart rate. Timepoint: Before and after the intervention, 1, 3, 5, 10 minutes after induction of anesthesia and then at 60 and 120 minutes. Method of measurement: Pulse oximetry device.;Arterial oxygen saturation. Timepoint: Before and after the intervention, 1, 3, 5, 10 minutes after induction of anesthesia and then at 60 and 120 minutes. Method of measurement: Pulse oximetry device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intensity of pain. Timepoint: At times 1, 3, 5, 10 minutes after induction of anesthesia and then at 60 and 120 minutes after induction of anesthesia. Method of measurement: Using criterion VAS. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBehzad Nazemroaya
Esfahan University of Medical Sciences
Outcome results
None listed