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Septorhinoplasty and Pain Score Course

I

Istinye University

Status

Not yet enrolling

Conditions

Visual Analogue Scale

Treatments

Procedure: septorhinoplasty

Study type

Observational

Funder types

Other

Identifiers

NCT07015229
haseki pacu cevahir

Details and patient eligibility

About

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.

Enrollment

78 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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,

Trial contacts and locations

0

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Central trial contact

ilke dolgun

Data sourced from clinicaltrials.gov

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