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Neramexane for Tinnitus

Primary Purpose

Tinnitus

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Neramexane
Placebo
Sponsored by
Merz Pharmaceuticals GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tinnitus

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • main inclusion criterion: persistent, subjective, uni- or bilateral tinnitus

Exclusion Criteria:

  • main exclusion criterion: intermittent or pulsatile tinnitus

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

Neramexane 25mg/d

Neramexane 50mg/d

Neramexane 75mg/d

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Change from baseline in tinnitus severity at the endpoint visit
Comparison of adverse events (type, severity, seriousness, frequency, relatedness) between treatment arms

Secondary Outcome Measures

Full Information

First Posted
November 29, 2006
Last Updated
March 10, 2011
Sponsor
Merz Pharmaceuticals GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT00405886
Brief Title
Neramexane for Tinnitus
Official Title
A Randomised, Double-Blind, Placebo-Controlled, Clinical Dose-Ranging Trial to Evaluate Efficacy and Safety of a NMDA Antagonist for Oral Administration in Patients With Subjective Tinnitus
Study Type
Interventional

2. Study Status

Record Verification Date
March 2011
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
March 2007 (Actual)
Study Completion Date
March 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Merz Pharmaceuticals GmbH

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Tinnitus is commonly referred to as "ringing of the ears" - the perception of sounds in the absence of an external source of acoustic signals. Tinnitus may represent a severe disease and symptoms include depression, sleeping difficulties, decreased sound tolerance and hearing loss. One hypothesis is that tinnitus is caused by an increased activity of NMDA glutamate and dysfunctional alpha9/alpha10 acetylcholine receptors in the inner ear and central nervous system. Neramexane may alleviate tinnitus symptoms due to its NMDA and alpha9/alpha10 nACh receptor blocking activity. The purpose of this study is to assess the safety and efficacy of Neramexane compared with placebo in patients with subjective tinnitus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tinnitus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
431 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Neramexane 25mg/d
Arm Type
Experimental
Arm Title
Neramexane 50mg/d
Arm Type
Experimental
Arm Title
Neramexane 75mg/d
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Neramexane
Intervention Description
Oral tablets, duration: 16 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Oral tablets, duration: 16 weeks
Primary Outcome Measure Information:
Title
Change from baseline in tinnitus severity at the endpoint visit
Time Frame
Week 16
Title
Comparison of adverse events (type, severity, seriousness, frequency, relatedness) between treatment arms
Time Frame
From baseline until week 20

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: main inclusion criterion: persistent, subjective, uni- or bilateral tinnitus Exclusion Criteria: main exclusion criterion: intermittent or pulsatile tinnitus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus Suckfüll, MD PhD Ass. Prof.
Organizational Affiliation
Ludwig-Maximilians - University of Munich
Official's Role
Study Chair
Facility Information:
City
Vienna
Country
Austria
City
Munich
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
21223542
Citation
Suckfull M, Althaus M, Ellers-Lenz B, Gebauer A, Gortelmeyer R, Jastreboff PJ, Moebius HJ, Rosenberg T, Russ H, Wirth Y, Krueger H. A randomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy and safety of neramexane in patients with moderate to severe subjective tinnitus. BMC Ear Nose Throat Disord. 2011 Jan 11;11:1. doi: 10.1186/1472-6815-11-1.
Results Reference
result
PubMed Identifier
21751942
Citation
Gortelmeyer R, Schmidt J, Suckfull M, Jastreboff P, Gebauer A, Kruger H, Wittmann W. Assessment of tinnitus-related impairments and disabilities using the German THI-12: sensitivity and stability of the scale over time. Int J Audiol. 2011 Aug;50(8):523-9. doi: 10.3109/14992027.2011.578591.
Results Reference
derived

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Neramexane for Tinnitus

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