A Multicenter, Double-blinded, Randomized, Placebo-controlled Trial to Compare the Effectiveness of Intratympanic Injections methylPREDnisolon Versus Placebo in the Treatment of Vertigo Attacks in MENière's Disease (PREDMEN Trial).

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Ménière's disease is an inner ear disorder in which patients suffer from attacks of vertigo, tinnitus and hearing loss. To date, it is unclear what the best treatment for this condition is. Giving injections in the inner ear with the adrenal cortical hormone methylprednisolone is a treatment that is already widely used, but still there is insufficient evidence in the effectiveness of this treatment. This multicenter trial compares a patient group which receives injections of methylprednisolone to a patient group which receives placebo injections. Subsequently, dizziness, tinnitus, hearing loss and quality of life will be assed and compared for the above mentioned groups, over a period of one year.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: t
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⁃ • Unilateral, definite MD according to the diagnostic criteria derived from the American Academy Otolaryngology Head and Neck Surgery, Classification Committee of the Bárány Society, European Academy of Otology and Neurotology and International Classification of Vestibular Disorders published in 2015 \[7\] (see Appendix 1):

⁃ Definite MD Two or more spontaneous episodes of vertigo, each lasting 20 minutes to 12 hours, AND Audiometrically documented low- to medium-frequency sensorineural hearing loss in one ear, defining the affected ear on at least one occasion before, during or after one of the episodes of vertigo, AND Fluctuating aural symptoms (hearing, tinnitus, or fullness) in affected ear (not better accounted for by another vestibular diagnosis)

• age \> 18 years at the start of the trial.

• ≥ 4 vertigo attacks over the last 6 months.

• willing to adhere to daily trial medications and the follow-up assessments.

Locations
Other Locations
Netherlands
Leiden University Medical Centre
RECRUITING
Leiden
Contact Information
Primary
Maud Boreel, MD
m.m.e.boreel@lumc.nl
+3171 526 9111
Backup
Babette van Esch, MD, PHD
b.f.van_esch@lumc.nl
+3171 526 9111
Time Frame
Start Date: 2023-10-01
Estimated Completion Date: 2027-02-01
Participants
Target number of participants: 148
Treatments
Active_comparator: Methylprednisolon
Intratympanal injection with Methylprednisolon 62.5 mg/ ml
Placebo_comparator: Placebo
Intratympanal injection with saline, natriumchloride 0.9%
Sponsors
Collaborators: HagaZiekenhuis, Medisch Spectrum Twente, Maasstad Hospital, Gelre Hospitals, Maastricht University Medical Center, ZonMw: The Netherlands Organisation for Health Research and Development
Leads: Leiden University Medical Center

This content was sourced from clinicaltrials.gov