RecruitingNot ApplicableNCT07568184

A Randomized Trial of Intratympanic Drug Delivery: Evaluating the Efficacy and Safety of Dexamethasone-Loaded Exosomes Versus Standard Therapy in Acute Sensorineural Hearing Loss.

A Phase II, Randomized Trial of Intratympanic Drug Delivery: Evaluating the Efficacy and Safety of Dexamethasone-Loaded Exosomes Versus Standard Therapy in Acute Sensorineural Hearing Loss.


Sponsor

Kafrelsheikh University

Enrollment

30 participants

Start Date

Apr 3, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Primary Objective To compare the efficacy of a single course of IT Exo-Dex versus conventional IT dexamethasone and exosome vehicle alone, as measured by the mean change in pure-tone average (PTA; 0.5, 1, 2, 4 kHz) from baseline to the 4-week post-treatment endpoint. Secondary Objectives 1. To determine the safety and tolerability profile of IT Exo-Dex. 2. To compare the rate of hearing recovery (defined as \>10 dB improvement in PTA or recovery to within 10 dB of contralateral ear) among the three treatment groups at 1, 4, and 12 weeks. 3. To assess changes in auditory function via Auditory Brainstem Response (ABR) thresholds and Otoacoustic Emissions (OAEs). 4. To characterize the pharmacokinetics and inner ear biodistribution of Exo-Dex using advanced imaging modalities (e.g., MRI with exosome-contrast agents in a sub-study cohort if applicable).


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria4

  • Adults aged 18-65 years.
  • Diagnosis of idiopathic SSNHL (≥30 dB sensorineural loss at three consecutive frequencies) within 14 days of symptom onset.
  • Failed initial standard systemic steroid therapy (e.g., oral prednisone 1 mg/kg/day for 7-14 days) or presented with contraindications to systemic steroids.
  • Willing and able to provide written informed consent.

Exclusion Criteria7

  • Identifiable cause of hearing loss (e.g., acoustic neuroma, Meniere's disease, trauma).
  • Pre-existing severe to profound hearing loss in the affected ear.
  • Active middle ear infection or tympanic membrane perforation.
  • History of autoimmune disease, coagulation disorders, or immunodeficiency.
  • Pregnancy or lactation.
  • Known hypersensitivity to dexamethasone or components of the exosome formulation.
  • Participation in another interventional clinical trial within 30 days.

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Interventions

DRUGexosomes derived from human umbilical cord mesenchymal stem cells

Exosomes (30-150 nm) are natural vesicles secreted by most cell types, playing crucial roles in intercellular communication via transport of proteins, lipids, and nucleic acids. As drug delivery vehicles, they offer intrinsic biocompatibility, low immunogenicity, and an innate ability to cross biological barriers.


Locations(1)

Kafrelsheikh University

Kafr ash Shaykh, Egypt, Egypt

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NCT07568184


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