Comparison of hemodynamic and respiratory changes in spinal anesthesia and general anesthesia in diagnostic laparoscopy in women. Other complications of anesthesia
Conditions
Interventions
Intervention 1: Control group:37 patients will be placed under general anesthesia with induction and maintenance of anesthesia with 1% intravenous propofol drug of Dongkook pharmaco company made in Ko
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Female with physical condition ASA(American Society of Anesthesiologists) class I or II In the age range of 60-18 years candidate for laparoscopic gynecological surgery Patient consent to study
Exclusion criteria
Exclusion criteria: Existence of any contraindications to regional anesthesia Sensitivity to local anesthetics Excessive obesity Accompanying systemic diseases such as any history of cardiovascular, pulmonary, hepatic, renal, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systolic and diastolic blood pressure. Timepoint: From the beginning of anesthesia to 30th minute,every 5 minutes and after that every 15minutes and in recovery section until discharging,every 10 minutes. Method of measurement: Mercury barometer.;Mean arterial pressure(MAP). Timepoint: From the beginning of anesthesia to 30th minute,every 5 minutes and after that every 15minutes and in recovery section until discharging,every 10 minutes. Method of measurement: Mercury barometer.;Heart rate. Timepoint: From the beginning of anesthesia to 30th minute,every 5 minutes and after that every 15minutes and in recovery section until discharging,every 10 minutes. Method of measurement: Counting in each minutes.;Saturation of peripheral oxygen. Timepoint: From the beginning of anesthesia to 30th minute,every 5 minutes and after that every 15minutes and in recovery section until discharging,every 10 minutes. Method of measurement: Via the Pulse Oximeter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Severity of postoperative nausea and vomiting. Timepoint: Every 5 minutes in recovery until discharge from recovery and transfer to ward. Method of measurement: scoring by (0=non, 1=nausea, 2=vomiting, 3=vomiting >2 times).;Severity of postoperative pain. Timepoint: Recovery and at 3, 6, 12,18 and 24 hours postoperatively. Method of measurement: Four Numerical Verbal Rating Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactReyhaneh Abri
Tabriz University of Medical Sciences
Outcome results
None listed