Septorhinoplasty and Pain Score Course
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: septorhinoplasty.
- Who it may be relevant to
- Registry conditions: Visual Analogue Scale. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
The Relationship of Pain Score Course and Analgesic Intervention Timing With Clinical Outcomes in the Postanesthetic Period After Septorhinoplasty
Overview
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.
Interventions
- Procedure septorhinoplasty
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.
Primary outcome measures
- visual analogue scale [Time frame: 60 minutes]
Eligibility criteria
Inclusion criteria
- 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,
- Being conscious and able to assess pain with VAS.
Exclusion criteria
- 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
- History of neurological or neuromuscular disease
- Having undergone revision septorhinoplasty or other revision surgery
- Patients with VAS≥4 during their follow-up in the postoperative,
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Publications
- Alshehri AA. Comparative Evaluation of Postoperative Pain Scores and Opioid Consumption in Septorhinoplasty After Administration of Single-Dose Preemptive Paracetamol and Ibuprofen: A Randomized Controlled Trial. Int Arch Otorhinolaryngol. 2023 Aug 4;27(3):e471-e477. doi: 10.1055/s-0042-1749386. eCollection 2023 Jul. PMID 37564463
- Perianez CAH, Castillo-Diaz MA, Barbosa MH, De Mattia AL. Pain Predictors in Patients in the Postanesthesia Care Unit. J Perianesth Nurs. 2024 Aug;39(4):652-658. doi: 10.1016/j.jopan.2023.11.010. Epub 2024 Feb 3. PMID 38310508
Identifiers
NCT: NCT07015229 · haseki pacu cevahir