Safety and Efficacy of Intratympanic Application of Dexamethasone Via Catheter in Patients With Sudden Hearing Loss
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|ClinicalTrials.gov Identifier: NCT00335920|
Recruitment Status : Completed
First Posted : June 12, 2006
Last Update Posted : February 5, 2008
|Condition or disease||Intervention/treatment||Phase|
|Sudden Deafness||Drug: Dexamethasone-dihydrogenphosphate (4mg/ml)||Phase 3|
Patients suffering from unilateral severe to profound sudden sensorineural hearing loss (ISSNHL) or anacusis with no or insufficient recovery after 12-21 days after onset will be treated for 14 days with Dexamethasone or placebo delivered intratympanically via a micro-catheter temporarily implanted into the round window niche and an external mini-pump.
Due to the relatively unknown risks of intratympanic treatment by catheter implantation, a significant spontaneous recovery rate and an existing standard therapy for ISSNHL in Germany (systemic glucocorticoids), patients will only be enrolled into the study if no or insufficient recovery of hearing threshold could be observed after initial systemic therapy.
The study will be carried out until 10 patients per group have been randomized regardless in which study center they have been randomized. After the last patient of these 10 patients per group has reached the endpoint an interim analysis will be done. The statistical estimation of the total number of subjects to be randomized will be completed after this interim analysis by the responsible statistician.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||23 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Prospective, Randomized, Double Blind, Placebo Controlled, Multicenter Study on the Safety and Efficacy of Continuous Infusion of Corticosteroid Delivered Via Catheter in Patients With Idiopathic Sudden Sensorineural Hearing Loss|
|Study Start Date :||October 2003|
|Actual Primary Completion Date :||July 2006|
|Actual Study Completion Date :||July 2007|
- Pure tone audiometric threshold
- Word recognition (speech audiometry)
- tinnitus improvement
- adverse events (worsening of hearing and/or vertigo and/or tinnitus, middle ear inflammation, pain)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00335920
|St. Vincentius Kliniken, Klinik für HNO Heilkunde|
|Karlsruhe, Germany, 76042|
|Department of Otorhinolaryngology, University of Tubingen|
|Tubingen, Germany, 72076|
|Ulm, Germany, 89081|
|Principal Investigator:||Hans-Peter Zenner, M.D.||Department of Otorhinolaryngology, University of Tubingen|
|Study Director:||Stefan K Plontke, M.D.||Department of Otorhinolaryngology, University of Tubingen|