Sudden Deafness, Sudden Sensorineural Hearing Loss
Conditions
Keywords
sudden deafness, SSNHL, migraine, topiramate, sudden sensorineural hearing loss
Brief summary
Migraine and sudden sensorineural hearing loss(SSNHL) are two related disorders. A systemic steroid is usually used to treat SSNHL but the role of migraine prophylaxis medication remained unknown. Mehdi Abouzari et al. found a better improvement when combining topiramate and nortriptyline with steroids in a retrospective study. However, a prospective study with randomization is needed to elucidate the efficacy of these agents. This is a clinical study using medication approved and currently prescribed in the clinic. The included patients were those who came to the clinic and were diagnosed with SSNHL within 14 days of onset. Those patients were asked whether they agreed to participate in this clinical trial. Patients who were diagnosed with SSNHL but were later found to be other diseases such as Meniere's disease and cerebellopontine angle will be excluded from this study. The involved patients were randomized divided into two groups. Both groups received systemic steroids with/without intratympanic steroids. The experimental group receives additional oral topiramate for 6 weeks. Follow-up time is at least 3 months. This study is multi-center. Location of the study is performed at Chang gung memorial hospital Linkou branch, Taipei branch, Taoyuan branch, and New Taipei Municipal Tucheng Hospital.
Detailed description
Once the patients were diagnosed with SSNHL, detailed information of the clinical trial will be introduced. If the patient agreed to participate, he/she will be randomized. The experimental group receives additional oral topiramate for 6 weeks. Both groups follow up at the clinic for at least 3 months. The pure tone audiometry and speech audiometry will be measured at the initial and end of follow-up. Patients who were later diagnosed with cerebellopontine angle tumors, stroke, or Meniere's disease, will be excluded from this study. The audiometry and other hearing outcomes will be analyzed at the end of the study. The treatment efficacy, and prognostic factors will be analyzed and reported. Data regarding adverse effects and drop-out will also be collected and reported.
Interventions
DRUGTopiramate
The topiramate arm receives additional oral topiramate for 6 weeks. The dose of topiramate is started from 25mg orally daily with the weekly escalation of 25mg to a maximum of 100mg.
Both groups receive a systemic steroid with/without intratympanic steroids as the standard treatment of SSNHL.
Sponsors
Chang Gung Memorial Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Masking description
This is an open-label study.
Intervention model description
Participants are assigned to one of two groups in parallel for the duration of the study.
Eligibility
Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age \> 20 * Confirmed diagnosis of unilateral sudden sensorineural hearing loss(SSNHL) * Treatment started 14 days within onset of SSNHL
Exclusion criteria
* Previous SSNHL history * Previous middle ear disorder such as chronic otitis media, or previous ear surgery * Meniere's disease and fluctuating hearing loss patients * Pregnancy or trying to become pregnant * Leukemia, hemodialysis, and patients who received chemotherapy before. * Previous head and neck radiotherapy * cerebellopontine angle tumors such as vestibular schwannoma * Patients with moderate to severe hepatic insufficiency * Patients with major depression disorder or suicide attempt * Patients with glaucoma
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Audiometry change | Baseline pure tone audiometry will be measured at the time of recruitment. The audiometry will be followed up 3 months after the initial recruitment. The audiometry change between two arms will be calculated and analyzed at the study completion. | The improvement rate and gain of pure tone audiometry (compare day 0 and day 84) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Audiometry change | The word recognition score will be measured at the time of recruitment(day 0) and end of study(day 84). The pure tone audiometry will be measured at day 56 and improvement would be calculated. | The improvement rate and gain of word recognition score (compare day 0 and day 84). The improvement rate and gain of pure tone audiometry (compare day 0 and day 56) |
Countries
Taiwan
Contacts
Primary ContactBANG-YAN ZHANG, MD.
Outcome results
None listed