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Recruiting NCT06291402

Nasal Packing Duration and Development of Pharyngitis After Septorhinoplasty Surgery

Observational Rhinitis

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Rhinitis. Basic parameters: 20 years — 40 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
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Nasal Packing Duration and Its Role in the Development of Pharyngitis After Septorhinoplasty Surgery: A Prospective Observational Study

Overview

Septoplasty or septal reconstruction is a corrective surgical procedure performed to straighten the nasal septum. It may be associated with numerous complications. To minimize these complications, both nasal cavities are frequently packed with different types of nasal packing. In our study we will try to find relationship between duration of nasal packing and postrhinoplasty sore throat and pharyngitis.

Detailed description

Nasal packing affects swallowing by different mechanisms. It may affect swallowing as a result of nasal congestion, constant mouth breathing, throat dryness and pharyngitis.

Postoperative sore throat causes patient dissatisfaction and poor pain control. Several interventions could be performed to reduce sore throat and pharyngitis and increase patient satisfaction , which may not be convenient for all patients, such as gargling or sprays

Primary outcome measures

  • Sore throat [Time frame: 48 hours postoperatively]
Secondary outcome measures (2)
  • Dysphagia [Time frame: 48 hours postoperatively]
  • Throat irritation [Time frame: 48 hours postoperatively]

Eligibility criteria

Inclusion criteria

  • ASA I and II patients
  • aged from 20 to 40 years old
  • undergo septorhinoplasty

Exclusion criteria

  • Bleeding disorders
  • Uncontrolled hypertension
  • Cardiovascular diseases
  • Uncontrolled diabetes mellitus
  • Collagen disorders
  • Pregnancy

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

Egypt · 1 center
  • Neveen Kohaf — Tanta

Identifiers

NCT: NCT06291402 · RC 34-1-2024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗