Condition 1: Patients undergoing abdominal surgery Like cholecystectomy. Condition 2: Patients undergoing abdominal surgery Like abdominal hernias. Condition 3: Patients undergoing abdominal surgery Like a hysterectomy. Retained cholelithiasis following cholecystectomy Incisional hernia without obstruction or gangrene Prolapse of vaginal vault after hysterectomy
Conditions
Interventions
Intervention 1: Intervention group: This clinical trial study will be performed on 80 candidates undergoing abdominal surgery by general anesthesia referring to the operating room of teaching hospital
Sponsors
Mazandaran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients undergoing elective abdominal surgery including abdominal hernia and open hysterectomy and open cystectomy Patients receiving general anesthesia ASA class 1 and 2 patients Surgical incisions above 5 cm Surgery time of at least one hour and maximum of 2.5 hours
Exclusion criteria
Exclusion criteria: Occurrence of any condition affecting the patient's normal anesthesia and surgery, such as excessive bleeding and cardiac arrest during surgery Having underlying diseases (thyroid, diabetes, cardiovascular disease and chronic hypertension) Receiving blood and blood products during surgery Intravenous fluids greater than 5 liters during surgery, temperatures above 37.5 ° C or less than 36.5 ° C before surgery Significant hypotension during surgery (20% blood pressure lower than before anesthesia) Endocrine Disorders Corticosteroid intake Non-steroidal analgesic and magnesium sulfate Fever, and addiction Prohibition on controlling body temperature through the tympanic membrane Lack of patient satisfaction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Central body temperature. Timepoint: Before Intervention - During Intervention - After Intervention. Method of measurement: Based on the temperature and using a tympan thermometer.;Shiver. Timepoint: During the intervention - after the intervention. Method of measurement: Will be reviewed according to the Crossley classification. Grade 1 = no shiver, grade 2 = slight shivering (straightening of hair, peripheral cyanosis without visible shake), grade 3 = moderate shivering (visible muscle shake in a group of muscles), grade 4 = severe shivering (muscle shake in All body muscles).;Recovery time. Timepoint: after surgery. Method of measurement: timer. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: Before intervention - During intervention - After intervention. Method of measurement: Systolic and diastolic blood pressure monitored using a millimeter of mercury.;Number of pulses. Timepoint: Before intervention - During intervention - After intervention. Method of measurement: Using the monitor on a per-minute basis.;Breath rate. Timepoint: Before intervention - During intervention - After intervention. Method of measurement: Using the monitor on a per-minute basis.;Percentage of arterial blood oxygen saturation. Timepoint: Before intervention - During intervention - After intervention. Method of measurement: Using a monitor based on percentages. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactTayebeh Azarmehr
Mazandaran University of Medical Sciences
Outcome results
None listed