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Dopamin agonista pramipexol hatása tinnitusra presbyacusisban

Dopamin agonista pramipexol hatása tinnitusra presbyacusisban

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2007-006271-37-HU
Enrollment
40
Registered
2007-12-05
Start date
2008-06-16
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tinnitus and old age presbycusis.

Interventions

Trade Name: MIRAPEXIN Product Name: Mirapexin Pharmaceutical Form: Tablet Pharmaceutical form of the placebo: Tablet Route of administration of the placebo: Oral use

Sponsors

Medical and Health Science Center, University of Debrecen Dept. of Otolaryngology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age over 50 years, Tinnitus, Presbycusis Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Conductive hearing loss Menier disease Other innear ear deafness Neuro degenerative disease Not controlled hypertension Cardiac decompensation

Design outcomes

Primary

MeasureTime frame
Main Objective: To study the putative efficacy of Mirapexin on tinnitus and presbycusis.;Secondary Objective: ;Primary end point(s): Hearing after 4 weeks and 12 weeks after one month treatment.

Countries

Hungary

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026