About this trial
The main aim of our study was to investigate the relationship between perioperative hypothermia and postoperative emergence agitation.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients with informed consent Elective planned cases
Patients between the ages of 18-65
American Society of Anesthesiologists ASA classification ASA 1-2 patients
Surgeries planned to last at least 30 minutes.
Disqualifiers
Patients who refuse to participate in the study,
patients who are considered for emergency surgery,
pediatric patients,
patients with peripheral vascular diseases or carotid stenosis,
Trial population
Patients who will be operated in ENT operating rooms in a tertiary education and research hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
surgery
Procedure/SurgeryENT surgery lasting more than half an hour
sedation scale
Procedure/SurgeryMeasurement of postoperative recovery with the Richmond agitation scale and the Riker sedation scale
Treatment groups
Trial outcomes
Primary outcomes
Relationship between hypothermia and emergence agitation
Comparison of recovery agitation rates in postoperative hypothermic and non-hypothermic patients
Secondary outcomes
Incidence of perioperative hypothermia
Incidence of hypothermia observed in the operating room and recovery room
Other outcomes
Comparison of agitation/sedation rates in hypothermic patients
Comparison of agitation/sedation rates in hypothermic patients will be compared by measuring percentages
Sponsors and contacts
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