Impact of nasal packing duration on sore throat after septorhinoplasty
Nasal Packing Duration and Its Role in the Development of Pharyngitis After Septorhinoplasty Surgery: A Prospective Observational Study
This study looks at how long nasal packing after nose surgery affects sore throat and discomfort to see if shorter packing times can help patients feel better.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 20 Years to 40 Years |
| Sex | All |
| Sponsor | Al-Azhar University Academic / other |
| Locations | 1 site (Tanta, Egypt) |
| Trial ID | NCT06291402 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the relationship between the duration of nasal packing following septorhinoplasty surgery and the development of postoperative sore throat and pharyngitis. The research aims to understand how nasal packing affects swallowing and throat discomfort, which can lead to patient dissatisfaction. By analyzing the effects of different packing durations, the study seeks to identify potential interventions to improve patient outcomes and satisfaction post-surgery.
Who should consider this trial
Good fit: Ideal candidates are ASA I and II patients aged 20 to 40 years who are scheduled for septorhinoplasty.
Not a fit: Patients with bleeding disorders, uncontrolled hypertension, cardiovascular diseases, uncontrolled diabetes, collagen disorders, or those who are pregnant may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved postoperative care and reduced throat discomfort for patients undergoing septorhinoplasty.
How similar studies have performed: While similar studies have explored postoperative complications in nasal surgeries, this specific focus on nasal packing duration and its effects on pharyngitis is relatively novel.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Tanta, Egypt
- Neveen Kohaf — Tanta, Egypt, Egypt (Recruiting)
Study contacts
- Principal investigator: Neveen Kohaf, ph.d — Al-Azhar University
- Study coordinator: Neveen Kohaf, Ph.D
- Email: nevenabdo@azhar.edu.eg
- Phone: +201060383012
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.