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Clinical Trial Summary

This study aimed to evaluate the effectiveness of silastic septal splint in reducing the rates of complications, decreasing the post-operative pain, and improving satisfaction in comparison to quilting suturing technique. Methods: A single center randomized controlled trial, including adult above the age of 18. A total of 50 participants who underwent septoplasty were enrolled and randomly assigned into two groups, Silastic group (n=25), and quilting group (n=25). Nasal obstruction severity was assessed by using an Arabic validated version of NOSE score, preoperatively then 3 days, one week and one month postoperatively. Post-operative complications were assessed at outpatient clinic 1 week and 1 month postoperatively. Pain was assessed by a 10-point numerical scales via phone call on the 3rd day postoperative.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04921462
Study type Interventional
Source King Abdulaziz Medical City
Contact
Status Completed
Phase N/A
Start date September 29, 2020
Completion date May 4, 2021

See also
  Status Clinical Trial Phase
Completed NCT04392583 - Safety and Performance of ENTACT Septal Staple System for Septoplasty
Recruiting NCT04020367 - Validation of a Process for the Manufacture of Stem Cells Isolated From the Nasal Cavity for Innovative Cell Therapy of Traumatized Peripheral Nerves N/A