Comparing methods to prevent complications after septoplasty
Comparative Study Between the Efficacy of Trans-Septal Quilting Sutures, Nasal Pack and Intranasal Silicon Splint in Endoscopic Septoplasty
This study is testing which of three methods—quilting sutures, nasal packing, or silicone splints—works best to prevent problems after surgery for a crooked nose.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 16 Years to 60 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta) |
| Trial ID | NCT06920368 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of three different techniques—trans-nasal quilting sutures, nasal packing, and intra-nasal silicon splinting—in preventing complications following endoscopic septoplasty. Septoplasty is performed to correct a deviated septum, but complications can arise post-operatively. The study will evaluate which method minimizes complications such as septal hematoma and improves patient quality of life. Healthy adults aged 16 to 60 with symptomatic deviated nasal septum will be included in the trial.
Who should consider this trial
Good fit: Ideal candidates are healthy adults aged 16 to 60 with symptomatic deviated nasal septum.
Not a fit: Patients with nasal polyposis, tumors, or those who have had previous septal surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and reduced complications for patients undergoing septoplasty.
How similar studies have performed: While there have been studies on septoplasty techniques, this specific comparison of methods is novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy adult patient of different ages from 16 to 60 year-old with symptomatic deviated nasal septum Exclusion Criteria: * Patient with nasal polyposis or nasal tumors or patients with sinusitis not responding to medical treatment. * Patient with previous septal operation * Patient who is planned to do partial inferior turbinectomy or turbinoplasty with septoplasty * Patients with contraindications for general surgery
Where this trial is running
Tanta
- Tanta University Hospitals — Tanta, Egypt (Recruiting)
Study contacts
- Principal investigator: Emad Mohamed Shehata, Professor — Tanta University Hospitals
- Study coordinator: Ahmed Yahia Ata, Master
- Email: ahmed179467_pg@med.tanta.edu.eg
- Phone: 0201018454445
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.