About this trial
To provide scientific contribution to more effective and timely pain management strategies in the postoperative period by evaluating the time-dependent course of pain scores and the effect of analgesic intervention timing on clinical outcomes in patients who underwent septorhinoplasty and who are followed in the postanesthetic care unit.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Being 18 years of age or older,
Being in ASA I-III class,
Having undergone septorhinoplasty surgery under general anesthesia under elective conditions,
Being monitored for at least 30 minutes in postoperative,
Disqualifiers
Patients who have undergone surgical procedures other than septorhinoplasty (e.g. laparoscopic, gynecological, orthopedic, etc.)
Inability to assess pain due to impaired consciousness, agitation, or sedation in the postoperative period
History of opioid derivatives or continuous analgesic use in the preoperative period
Cognitive impairment, psychiatric disease at a level that prevents communication, severe visual or hearing impairment
Trial population
Patients aged 18-65 years with ASA 1-3 who underwent elective septorhinoplasty
Trial design
Cohort
Prospective
Treatments tested in this trial
septorhinoplasty
Procedure/SurgeryTo provide scientific contribution to more effective and timely pain management strategies in the postoperative period by evaluating the time-dependent course of pain scores and the effect of analgesic intervention timing on clinical outcomes in patients who underwent septorhinoplasty and who are followed in the postanesthetic care unit.
Treatment groups
Trial outcomes
Primary outcomes
visual analogue scale
0:no pain, 10:worst pain
Locations
Sponsors and contacts
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Istinye University
Lead sponsor
Haseki Training and Research Hospital
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: