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NCT Number: NCT07015229

Septorhinoplasty and Pain Score Course

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.

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Key information

Conditions

Visual Analogue Scale

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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,

Treatment and study plan

septorhinoplasty

Procedure

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 outcomes

  1. visual analogue scale

    Time frame: 60 minutes

    0:no pain, 10:worst pain

Study contacts

Contact information is provided by the study sponsor or research team.

ilke dolgun

CONTACT

[email protected]

+905555485632

Sponsors and collaborators

Lead sponsor

Istinye University

Other

Registry information

Official study title

The Relationship of Pain Score Course and Analgesic Intervention Timing With Clinical Outcomes in the Postanesthetic Period After Septorhinoplasty

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 11, 2025
Registry last updated
Jun 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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