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Sudden Deafness Treatment Trial (SSNHL)

This study is currently recruiting participants.
Verified by National Institute on Deafness and Other Communication Disorders (NIDCD), August 2008

Sponsored by: National Institute on Deafness and Other Communication Disorders (NIDCD)
Information provided by: National Institute on Deafness and Other Communication Disorders (NIDCD)
ClinicalTrials.gov Identifier: NCT00097448
  Purpose

This trial aims to compare the efficacy of oral prednisone vs. methylprednisolone injected into the middle ear for the treatment of moderate-to-severe, sudden sensorineural hearing loss (inner ear hearing loss affecting one ear that occurs over less than 72 hours).


Condition Intervention Phase
Sudden Deafness
Drug: prednisone
Drug: methylprednisolone sodium succinate
Phase II

Genetics Home Reference related topics:   nonsyndromic deafness   

MedlinePlus related topics:   Hearing Disorders and Deafness   

ChemIDplus related topics:   Methylprednisolone    Methylprednisolone Sodium Succinate    Prednisone    Succinic acid   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study
Official Title:   Sudden Hearing Loss Multicenter Treatment Trial

Further study details as provided by National Institute on Deafness and Other Communication Disorders (NIDCD):

Primary Outcome Measures:
  • hearing improvement [ Time Frame: 6 months ] [ Designated as safety issue: Yes ]

Estimated Enrollment:   254
Study Start Date:   December 2004
Estimated Study Completion Date:   March 2009
Estimated Primary Completion Date:   December 2008 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1
Nineteen days of oral prednisone
Drug: prednisone
Oral, 19 days
2: Experimental
Four doses of methylprednisolone sodium succinate delivered by injection to the middle ear over 2 weeks
Drug: methylprednisolone sodium succinate
Four intratympanic injections delivered to the middle ear over 2 weeks

Detailed Description:

Sudden deafness is believed to affect 1:5000 people yearly. The cause is unknown. Spontaneous improvement is seen in approximately 20% of subjects. Improvement is seen in approximately 60% of subjects treated promptly with oral corticosteroids. Anecdotal case reports and uncontrolled case series have suggested the intratympanic corticosteroids may work as well or better than oral treatment. The risks of oral prednisone are well-known. In theory, intratympanic treatment should achieve a higher drug concentration at the target (inner ear) with less risk of systemic side effects. This study is a head-to-head comparison of oral prednisone vs. intratympanic methylprednisolone for primary treatment of idiopathic sudden deafness. The study is designed as a non-inferiority trial testing that hypothesis that intratympanic methylprednisolone is not inferior to oral prednisone treatment. Subjects assigned to the oral treatment arm receive 14 days of high dose prednisone (60mg/day) followed by a 5-day taper. Subjects assigned to the intratympanic treatment arm receive 4 doses of methylprednisolone injected into the middle twice weekly for two weeks. The primary outcome measure is hearing as measured by pure tone audiometry. Secondary outcomes include word recognition hearing levels and safety issues of local vs. systemic steroid side-effects and pain.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Men/women 18 years and older in good health
  • Unilateral sensorineural hearing loss developing within 72 hours (SSNHL)
  • Pure Tone Average (PTA) (500, 1000, 2000, 4000 Hz) >/= 50 dB in the affected ear, with the affected ear >/= 30 dB worse than contralateral ear in at least one of the four frequencies
  • Symmetric hearing prior to onset of SSNHL
  • Hearing loss must be idiopathic
  • Hearing loss must have occurred within the past 14 days
  • Must be able to read or write English or Spanish

Exclusion Criteria:

SYSTEMIC DISEASE

  • >21 days prior oral steroid treatment within preceding 30 days
  • History of tuberculosis (TB) or positive PPD
  • Insulin-dependent diabetes mellitus
  • History of rheumatic disease, e.g., rheumatoid arthritis, scleroderma, lupus, etc.
  • Serious psychiatric disease or psychiatric reaction to corticosteroids
  • History of heart disease or transient ischemic attacks (TIAs)
  • Prior treatment with chemotherapeutic or immunosuppressive drugs
  • Pancreatitis
  • Active peptic ulcer disease or history of gastrointestinal bleeding
  • History of HIV, Hepatitis B or C
  • Chronic kidney failure
  • Alcohol abuse
  • Active shingles
  • Severe osteoporosis or non-surgical aseptic necrosis of the hip

OTOLOGIC DISEASE

  • Prior history of SSNHL
  • History of fluctuating hearing loss
  • History of Meniere's disease
  • History of chronic ear infection
  • History of otosclerosis
  • History of ear surgery (except childhood pressure equalization [pe] tubes)
  • History of congenital hearing loss
  • History of trauma immediately preceding onset of SSNHL
  • History of syphilitic hearing loss
  • History of genetic/hereditary hearing loss
  • Skull, facial, or temporal bone anomalies
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00097448

Locations
United States, California
University of California San Diego     Recruiting
      San Diego, California, United States, 92103-8895
      Contact: Sharon Lindebak, MN, PA-C     858-657-6836     slindebak@ucsd.edu    
      Principal Investigator: Jeffrey P. Harris, MD, PhD            
House Ear Institute     Recruiting
      Los Angeles, California, United States, 90057
      Contact: Roberta Leyvas     213-273-8025     rleyvas@hei.org    
      Principal Investigator: William H Slattery, III, MD            
United States, Florida
University of Florida, College of Medicine     Recruiting
      Gainesville, Florida, United States, 32610
      Contact: Carrie R Reed     352-273-5171     carrie.reed@ent.ufl.edu    
      Principal Investigator: Patrick J Antonelli, MD            
United States, Iowa
University of Iowa     Recruiting
      Iowa City, Iowa, United States, 52242-1078
      Contact: Deborah Strike, BSN, RN     319-356-3345     deborah-strike@uiowa.edu    
      Principal Investigator: Bruce J. Gantz, MD            
      Sub-Investigator: Marlan R. Hansen, MD            
United States, Maryland
Johns Hopkins University     Recruiting
      Baltimore, Maryland, United States, 21287-0910
      Contact: Nancy Smith, PA-C     866-240-2576     nsmith2@jhmi.edu    
      Principal Investigator: John P. Carey, MD            
      Sub-Investigator: Charles Della Santina, MD, PhD            
United States, Massachusetts
Massachusetts Eye & Ear Infirmary     Recruiting
      Boston, Massachusetts, United States, 02114
      Contact: Mary L. Bartley, RN, BA     866-573-3628     mary_bartley@meei.harvard.edu    
      Principal Investigator: Steven D. Rauch, MD            
      Sub-Investigator: Daniel J. Lee, MD            
University of Massachusetts Medical School     Recruiting
      Worcester, Massachusetts, United States, 01655
      Contact: Karen Longtine, BS, RN, CCRC     508-722-0546     Karen.Longtine@umassmed.edu    
      Principal Investigator: Richard Gacek, MD            
United States, Michigan
University of Michigan     Recruiting
      Ann Arbor, Michigan, United States, 48109-0312
      Contact: Laura Eldred     734-764-6106     leldred@umich.edu    
      Principal Investigator: Steven A. Telian, MD            
      Sub-Investigator: Hussam El-Kashlan, MD            
Michigan Ear Institute     Recruiting
      Farmington Hills, Michigan, United States, 48334
      Contact: Cathy Bathurst, RN     248-865-4135     cbathurst53@yahoo.com    
      Principal Investigator: Seilesh Babu, MD            
United States, Missouri
Washington University School of Medicine     Recruiting
      St. Louis, Missouri, United States, 63110
      Contact: Belinda Sinks, MA     314-362-7546     sinksb@ent-wustl.edu    
      Principal Investigator: Joel A Goebel, MD            
United States, New York
New York University School of Medicine     Recruiting
      New York, New York, United States, 10016
      Contact: Dorline Jean, RN     212-263-7488     D.Jean@med.nyu.edu    
      Principal Investigator: Paul E. Hammerschlag, MD            
      Sub-Investigator: J. Thomas Roland, MD            
New York Eye and Ear Infirmary     Recruiting
      New York, New York, United States, 10003
      Contact: Nina Suslina, BS     212-979-4082     nsuslina@nyee.edu    
      Contact: Glorimel Casambre, BS     212-353-5776     gcasambre@nyee.edu    
      Principal Investigator: Christopher Linstrom, MD            
      Sub-Investigator: George Alexiades, MD            
      Sub-Investigator: Ana Kim, MD            
United States, Ohio
The Cleveland Clinic     Recruiting
      Cleveland, Ohio, United States, 44195
      Contact: Michelle A. Crespo, RN, BSN     216-444-5029     crespom@ccf.org    
      Principal Investigator: Gordon B. Hughes, MD            
      Sub-Investigator: Peter C. Weber, MD            
United States, Texas
University of Texas Southwestern Medical Center     Recruiting
      Dallas, Texas, United States, 75390
      Contact: Barbara Staves     214-648-9793     Barbara.staves@utsouthwestern.edu    
      Principal Investigator: Brandon Isaacson, MD            
Baylor College of Medicine     Recruiting
      Houston, Texas, United States, 77030
      Contact: Sharon Congdon     713-798-5819     scongdon@bcm.tmc.edu    
      Principal Investigator: Jeffrey T Vrabec, MD            
Canada, Ontario
London Health Sciences Center-University Hospital, University of Western Ontario     Recruiting
      London, Ontario, Canada, N6A 5A5
      Contact: Francie Si     519-685-8500 ext 55415     francie.si@lhsc.on.ca    
      Principal Investigator: Lorne S Parnes, MD            
      Sub-Investigator: Duncan L MacRae, MD            

Sponsors and Collaborators

Investigators
Principal Investigator:     Steven Rauch, MD     Massachusetts Eye and Ear Infirmary    
  More Information


Related Info  This link exits the ClinicalTrials.gov site
 

Responsible Party:   Massachusetts Eye and Ear Infirmary ( Steve D. Rauch, MD, Principal Investigator )
Study ID Numbers:   DC006296, 03-11-055
First Received:   November 23, 2004
Last Updated:   August 1, 2008
ClinicalTrials.gov Identifier:   NCT00097448
Health Authority:   United States: Federal Government;   United States: Food and Drug Administration

Keywords provided by National Institute on Deafness and Other Communication Disorders (NIDCD):
sudden hearing loss  
unilateral sudden sensorineural hearing loss  
sudden sensorineural hearing loss  
sudden unilateral hearing loss  

Study placed in the following topic categories:
Sensation Disorders
Prednisone
Otorhinolaryngologic Diseases
Methylprednisolone
Hearing Loss, Sudden
Sensorineural hearing loss
Methylprednisolone acetate
Prednisolone acetate
Hearing Loss, Sensorineural
Hearing Loss, Unilateral
Ear Diseases
Signs and Symptoms
Deafness
Hearing Disorders
Prednisolone
Neurologic Manifestations
Hearing Loss
Methylprednisolone Hemisuccinate

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Nervous System Diseases
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists
Gastrointestinal Agents
Antiemetics
Hormones
Neuroprotective Agents
Protective Agents
Glucocorticoids
Pharmacologic Actions
Autonomic Agents
Therapeutic Uses
Peripheral Nervous System Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on September 19, 2008




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