Overview
The goal of this clinical trial is to investigate if a 3-dimensional fabricated nasal mesh works to close nasal septal perforations. Under general anesthesia, during nasal septal perforation repair surgery, the investigator will place the mesh between the elevated mucoperichondrial flaps opposite the site of the perforation and confirm its original position at both sides under nasal endoscope. Endoscopic examination for septal mucosa status will be done monthly for a three months follow up period.
Eligibility
Inclusion Criteria:
- Patients undergoing nasal septal perforation repair surgery.
Exclusion Criteria:
- Patients with known allergy to polycaprolactone.
- Pregnancy or lactation.