Bleeding. Nasal congestion
Conditions
Interventions
Intervention 1: First intervention group: This group will be performed with the participation of 30 patients who are candidates for septorhinoplasty surgery
After anesthesia, the participants will receive artificial respiration 16 times per minute
Finally, the amount of bleeding will be measured. Intervention 2: Second intervention group: This group will be performed with the participation of 30 patients who are candidates for septorhinoplasty
After anesthesia, the participants will receive artificial respiration 10 times per minute
Finally, the amount of bleeding will be measured. Intervention 3: Control group: This group will be performed with the participation of 30 patients who are candidates for septorhinoplasty surgery
After anesthesia, the participants will receive artificial respiration 12 times per minute
Finally, the amount of bleeding will be measured.
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients with American Society of Anesthesiologists (ASA) Class II and I Septorhinoplasty surgery candidate
Exclusion criteria
Exclusion criteria: Patients with lung diseases (asthma and allergy) Body mass index above 40 kg/m2 Patients with electrolyte disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bleeding. Timepoint: It will be measured continuously during the surgery (from the beginning to the end of the surgery). Method of measurement: Bleeding is measured by the sum of the blood in the Saxen bottle and blood-soaked gauze. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehdi Khanbabayi Gol
Tabriz University of Medical Sciences
Outcome results
None listed