Context: Idiopathic Sudden Sensorineural Hearing Loss (ISSHL) is a rapid-onset, sensorineural hearing loss of unknown etiology. It is one of the most common ENT emergencies, with spontaneous recovery occurring in 32% to 65% of cases. Treatment remains controversial, and the need for treatment itself is debated. Oral corticosteroids (OCS) are commonly used as first-line therapy, although they may have short-term side effects. Intratympanic corticosteroid injections (ITCIs) are an option for patients with contraindications to OCS or as a salvage treatment. The most recent Cochrane review includes three placebo-controlled studies on OCS efficacy (totaling 267 patients): two found no superiority of OCS, while one showed improvement in hearing. These studies are inconsistent and present methodological biases. Therefore, a sufficiently powered study is needed to assess OCS efficacy and establish clear treatment recommendations for ISSHL. Objectives: Primary Objective: To demonstrate the equivalence of OCS as first-line treatment for ISSHL compared to no treatment, in terms of hearing recovery between days 7 and 10. Secondary Objectives: To assess the effect of OCS versus no treatment on tinnitus, and hearing recovery based on initial severity of ISSHL. To evaluate hearing recovery in patients treated with rescue ITCIs. In the absence of equivalence, to investigate the superiority of OCS over no treatment. Methods: This multicenter, randomized, controlled equivalence trial will include two arms, each with 215 patients: one receiving OCS and the other a no-treatment control. In the absence of early hearing improvement, ITCIs will be administered regardless of study arm. Perspective: The goal is to clarify the role of OCS in treating ISSHL and guide the development of updated treatment recommendations.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
430
Study of the Standard of care versus Placebo
Control
CHU de Besançon
Besançon, France
Early hearing recovery
Hearing recovery defined by (composite criterion) : * Gain of at least 10dB in pure tone average (PTA) on pure tone audiometry compared with initial PTA in dB, * or \> 10% improvement in intelligibility threshold on speech audiometry, compared with initial intelligibility threshold
Time frame: From enrollment to 10 +/- 2 days
Medium-term hearing recovery
Medium-term hearing recovery: * Gain of at least 10dB in pure tone average (PTA) on pure tone audiometry compared with initial PTA in dB, * or \> 10% improvement in intelligibility threshold on speech audiometry, compared with initial intelligibility threshold
Time frame: At 1 month and 3 months after enrollment
Tinnitus handicap
Change in tinnitus-related disability assessed by the Tinnitus Handicap Index (THI) score between inclusion and D10, M1, and M3.
Time frame: At 10 days, 1 month and 3 months after enrollment
Medium-term hearing recovery in patients without early recovery and treated with salvage trans-tympanic injections.
Hearing recovery defined by (composite criterion) : * Gain of at least 10dB in pure tone average (PTA) on pure tone audiometry compared with initial PTA in dB * or \> 10% improvement in intelligibility threshold on speech audiometry, compared with initial intelligibility threshold
Time frame: At 1 month and 3 months after enrollment
Subgroup analysis based on initial severity
Subgroup analysis according to initial PTA ≥ 70dB or \<70dB
Time frame: At 10 days, 1 month and 3 months after enrollment
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