Septorhinoplasty and Pain Score Course

NCT ID: NCT07015229

Last Updated: 2025-06-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

78 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-25

Study Completion Date

2026-01-20

Brief Summary

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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.

Detailed Description

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Conditions

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Visual Analogue Scale

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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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.

Intervention Type PROCEDURE

Eligibility Criteria

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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,
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istinye University

OTHER

Sponsor Role lead

Responsible Party

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İlke Dolgun

assoc. prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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ilke dolgun

Role: CONTACT

+905555485632

References

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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.

Reference Type RESULT
PMID: 37564463 (View on PubMed)

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.

Reference Type RESULT
PMID: 38310508 (View on PubMed)

Other Identifiers

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haseki pacu cevahir

Identifier Type: -

Identifier Source: org_study_id

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