Septorhinoplasty and Pain Score Course
ConditionVisual Analogue Scale
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorIstinye University
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
Qualifiers
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 design
Treatments tested in this trial
- septorhinoplasty
Treatment groups
No treatment groups listed
Locations
Sponsors and collaborators
Istinye University
Lead sponsor
Haseki Training and Research Hospital
Sponsor institution
Source ClinicalTrials.gov