A Single-blinded Randomised Trial Evaluating the Efficacy of Chitosan-dextran (Chitodex) Gel Versus Gelfoam Sponge Instillation Within the Middle Ear and External Auditory Canal During Tympanoplasty Surgery
The general purpose of this study is to compare Chitosan-dextran (Chitodex) gel versus current standard of care, Gelfoam, as a middle ear (ME) and external auditory canal (EAC) packing agent as part of tympanoplasty, ossiculoplasty and mastoidectomy procedures.
• Individuals who have otoscopic evidence of tympanic membrane perforation that is also confirmed by tympanometry (Defined as a Type B tympanogram, with elevated EAC volume) AND
‣ The TM perforation is associated with at least 15dB of conductive hearing loss on the affected side AND
⁃ Are indicated to undergo closure of the perforation via tympanoplasty surgery
• OR Individuals who are indicated for ossiculoplasty due to ossicular chain disruption and its sequelae
• OR Individuals who are indicated for mastoidectomy for COM or its sequelae eg cholesteatoma
• Demonstrate healthy, dry middle ear mucosal cavities at time of surgery AND
• Are 18 years of age or over AND
• Are able to give written informed consent AND
• Are committed to returning for post-operative assessments at 2 and 6 weeks post-op, 3-, and 6- months post-op