Evaluation of The Relationship Between Perioperative Hypothermia and Emergence Agitation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorKocaeli City Hospital

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • surgery

    Procedure/Surgery

    ENT surgery lasting more than half an hour

  • sedation scale

    Procedure/Surgery

    Measurement of postoperative recovery with the Richmond agitation scale and the Riker sedation scale

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: Group A2 interventions
Group B: Group B2 interventions

Trial outcomes

Primary outcomes

1

Relationship between hypothermia and emergence agitation

Comparison of recovery agitation rates in postoperative hypothermic and non-hypothermic patients

Time frame
first postoperative hour

Secondary outcomes

1

Incidence of perioperative hypothermia

Incidence of hypothermia observed in the operating room and recovery room

Time frame
Between the first 1 hour preoperatively and the first 1 hour postoperatively

Other outcomes

1

Comparison of agitation/sedation rates in hypothermic patients

Comparison of agitation/sedation rates in hypothermic patients will be compared by measuring percentages

Time frame
Between the first 1 hour preoperatively and the first 1 hour postoperatively

Sponsors and contacts

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