Chitogel versus Hydrogel on wound healing and patient experience following endosopic sinus surgery

Not Applicable

Withdrawn

• Conditions: Surgery - Other surgery; endoscopic sinus surgery; chronic rhinosinusitis; Respiratory - Other respiratory disorders / diseases

• Registration Number: ACTRN12621001336875
• Lead Sponsor: orth Shore Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-10-05
• Last Update Posted: 24 April 2023

Recruitment & Eligibility

• Status: Withdrawn
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients undergoing bilateral Functional ESS for CRS

Exclusion Criteria

Allergy to shellfish
Pregnancy/breast feeding
Previous sinus surgery

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post operative endoscopic degree of adhesion[2 weeks and 3 months post intervention commencement];Post operative endoscopic degree of crusting[2 weeks and 3 months (primary) post intervention commencement];Post operative endoscopic degree of granulations[2 weeks and 3 months (primary) post intervention commencement]

Secondary Outcome Measures

Name	Time	Method
Post operative endoscopic degree of mucosal oedema[2 weeks and 3 months post intervention commencement];Post operative endoscopic evidence of infection[2 weeks and 3 months post intervention commencement];Patient experience will be assessed with a subjective symptom score using the Sino–Nasal Outcome Test (SNOT–22)[3 months post commencement of intervention]