Efficacy and Safety of Hydroxychloroquine in the Treatment of Sudden Sensorineural Hearing Loss

Sudden sensorineural hearing loss (SSNHL) significantly affects a patient's social and interpersonal interactions. It presents as an abrupt decrease in hearing, usually within a matter of hours or days. SSNHL typically impacts one ear and can range in severity, sometimes resulting in total deafness. In clinical settings, steroids are the predominant treatment for SSNHL. Yet, the outcomes for patients undergoing steroid therapy for SSNHL can differ substantially. Hydroxychloroquine, a derivative of chloroquine, is a medication that has gained attention for its potential role in modulating the immune response. Our study hypothesized that hydroxychloroquine could help the hearing recovery during the steroid treatment for SSNHL.

In this project, we will enroll two groups of subjects for our study.

• Experimental group: Treatment with oral prednisolone (5 mg) for 14 days (high dosage 1 mg/kg/day for 7 days and gradually taper in the next week) and hydroxychloroquine for 60 days (400 mg/day)
• Control group: Treatment with oral prednisolone (5 mg) for 14 days (high dosage 1 mg/kg/day for 7 days and gradually taper in the next week)

A. Primary endpoint:

The primary outcome measure for this study is the change in pure tone audiogram (PTA) in the affected ear from screening until 3 months. The PTA will be calculated as the arithmetic mean of air conduction thresholds at the frequency of 0.5k, 1k, 2k, and 4 kHz.

B. Secondary endpoints:

• the change in PTA in the bilateral ear from screening until one week, two weeks, one month, and two months
• change in word recognition score (WRS) in the bilateral ear from screening to one week, two weeks, one month, two months and three months
• The grade of hearing recovery by Siegel's criteria from screening to 3 months
• Percentage of recovery from screening until 3 months
• change in bilateral tinnitus severity (evaluted by VAS and THI) from screening to one month, 2 months and 3 months

Inclusion criteria

• Unilateral idiopathic sudden sensorineural hearing loss ≥ 30 dB in at least 3 consecutive frequencies, compared to the contralateral ear, within 3 days
• Enrollment has to be accomplished within 14 days after SSNHL onset
• Male or female aged ≥ 18 to 70 years
• Ability to understand and follow the study protocol

Exclusion criteria

• Pregnant or breast-feeding female
• positive pregnancy test before receiving the study drug
• Due to a history of physical efforts suspected perilymph fistula or membrane rupture.
• Previously existing, known retrocochlear hearing loss
• Any history of any ear operation or chronic inflammatory disease of middle ear in the past one year
• History of blunt or penetrating ear trauma, head trauma, barotrauma, or acoustic trauma immediately preceding SSHL.
• History of Meniere's disease, autoimmune hearing loss, radiation-induced hearing loss, endolymphatic hydrops, and otosclerosis.
• History of chronic inflammatory diseases or autoimmune diseases
• Prior chemotherapy or treatment with immunosuppressant drugs
• Patients on renal dialysis
• Patients with history of retinopathy, or are using drugs that could induce retinopathy, such as Tamoxifen
• History of allergy to hydroxychloroquine
• Patients who are contraindicated with oral steroid treatment