Efficacy and safety of systemic, high-dose glucocorticoid therapy for idiopathic sudden sensorineural hearing loss Study protocol for a three-armed, randomized, triple-blind, multicenter trial (HODOKORT)

被引:11
|
作者
Plontke, Stefan K. [1 ]
Girndt, Matthias [2 ]
Meisner, Christoph [3 ]
Boeselt, Iris [4 ]
Ludwig-Kraus, Beatrice [5 ]
Richter, Michael [4 ]
Rahne, Torsten [1 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Dept Otorhinolaryngol Head & Neck Surg, Ernst Grube Str 40, D-06120 Halle, Saale, Germany
[2] Martin Luther Univ Halle Wittenberg, Dept Med, Halle, Saale, Germany
[3] Robert Bosch Krankenhaus, Robert Bosch Soc Med Res, Stuttgart, Germany
[4] Martin Luther Univ Halle Wittenberg, Coordinat Ctr Clin Trials, Halle, Saale, Germany
[5] Univ Hosp Halle, Cent Lab, Halle, Saale, Germany
关键词
Corticosteroids; Dexamethasone; Glucocorticoids; Humans; Idiopathic; Prednisolone; Randomized controlled trial; Steroids; Sudden hearing loss; STEROID-THERAPY; METAANALYSIS; PLACEBO; HYPERTENSION; DEAFNESS; FAILURE;
D O I
10.1007/s00106-022-01184-8
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background Systemic glucocorticosteroids ("steroids") are widely used worldwide as a standard of care for primary therapy of idiopathic sudden sensorineural hearing loss (ISSHL). The German ISSHL guideline recommends high-dose steroids without evidence from randomized controlled trials (RCTs) and refers solely to retrospective cohort studies. This RCT aims to assess the efficacy (improvement in hearing) and safety (especially systemic side effects) of high-dose steroids versus standard of care (standard dose systemic steroids) for the treatment of unilateral ISSHL, when given as a primary therapy. Methods The study is designed as a multicenter (approximately 40 centers), randomized, triple-blind, three-armed, parallel group, clinical trial with 312 adult patients. The interventions consist of 5 days of 250 mg/day intravenous prednisolone (intervention 1) + oral placebo, or 5 days of 40 mg/day oral dexamethasone (intervention 2) + intravenous placebo. The control intervention consists of 60 mg oral prednisolone for 5 days followed by five tapering doses + intravenous placebo. The primary efficacy endpoint is the change in hearing threshold in the three most affected contiguous frequencies between 0.25 and 8 kHz 1 month after ISSHL. Secondary endpoints include further measures of hearing improvement including speech audiometry, tinnitus, quality of life, blood pressure, and altered glucose tolerance. Discussion There is an unmet medical need for an effective medical therapy of ISSHL. Although sensorineural hearing impairment can be partially compensated by hearing aids or cochlear implants (CI), generic hearing is better than using hearing aids or CIs. Since adverse effects of a short course of high-dose systemic corticosteroids have not been documented with good evidence, the trial will improve knowledge on possible side effects in the different treatment arms with a focus on hyperglycemia and hypertension.
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收藏
页码:30 / 44
页数:15
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