A Study on the Effect of Cilostazol in Patients With Chronic Tinnitus
NCT ID: NCT01378650
Last Updated: 2014-05-22
Study Results
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Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2011-07-31
2013-06-30
Brief Summary
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2. Characteristics of the clinical research drug, cilostazol Cilostazol inhibits phosphodiesterase type 3 (PDE3) selectively and increases amount of cAMP by inhibition of degradation of cyclic adenosine monophosphate(cAMP). cAMP again by increasing the active form of PKA suppress the production of blood clots and increase blood flow by expanding blood vessels. Anti-platelet activity and vasodilatation effect of cilostazol have been used for improvement of diabetic peripheral vascular disorders and suppression of stroke recurrence. Previous studies reported that by increasing the activity of NO and PKA, the blood flow of stria vascularis and cochlear hair cells can be improved. These studies implies that cilostazol, which causes inhibition of PDE3 and increase of PKA, can have a potential effect on improvement of tinnitus by increase of blood flow to peripheral cochlear cells. Thus, we hypothesized that cilostazol, which has been widely used for enhancing peripheral blood flow, can bring improvement of tinnitus by causing better peripheral blood flow of cochlea.
3. The aim of the study We planned this study to validate the assumptions of the background. The aim of our study is whether administration of cilostazol can improve tinnitus in terms of subjective degree of symptoms in chronic tinnitus patients.
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Detailed Description
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* Determination of eligibility by history taking, physical examination, pure tone audiometry, speech audiometry, and distortion product otoacoustic emission test.
* Randomization by random sequence generation
* Administration : cilostazol 100mg Bid 4 weeks for the study group and placebo tablet Bid 4 weeks for the control group.
* Evaluation battery: questionnaires (tinnitus handicap inventory, visual analogue scale, Quality of life SF-36)
* Time of evaluation : pre-administration, 2 weeks after administration, 4 week after administration
* Monitoring of side effects
2. Evaluation of treatment response - Statistical analysis of scores of questionnaires using SPSS K12.0 (paired t-test for changes of each group and Mann-Whitney U test for comparing the mean scores of two groups)
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Cilostazol group
Administration of Cilostazol 100mg twice a day for 4 weeks
Cilostazol
Administration of Cilostazol 100mg twice a day for 4 weeks
Placebo group
placebo drug twice a day for 4 weeks.
Placebo
placebo one tablet matching for cilostazol twice a day for 4 weeks.
Interventions
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Cilostazol
Administration of Cilostazol 100mg twice a day for 4 weeks
Placebo
placebo one tablet matching for cilostazol twice a day for 4 weeks.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Unilateral or bilateral tinnitus
* Chronic tinnitus lasting more than 3 months
* Initial visual analogue scale of tinnitus \>3
Exclusion Criteria
* Associated other inner ear diseases such as Meniere's disease
* Objective or pulsatile tinnitus
* Contraindication to anti-platelet drug
* Any cardiac disease
* Bleeding tendency and major operation within 3 months
* Breastfeeding
* Pregnancy
20 Years
ALL
No
Sponsors
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Korea Otsuka Pharmaceutical Co., Ltd.
INDUSTRY
Jong Woo Chung
OTHER
Responsible Party
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Jong Woo Chung
MD
Principal Investigators
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Jong Woo Chung, M.D.
Role: PRINCIPAL_INVESTIGATOR
Asan Medical Center
Locations
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Asan Medical Center
Seoul, , South Korea
Countries
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References
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Mazurek B, Haupt H, Szczepek AJ, Sandmann J, Gross J, Klapp BF, Kiesewetter H, Kalus U, Stover T, Caffier PP. Evaluation of vardenafil for the treatment of subjective tinnitus: a controlled pilot study. J Negat Results Biomed. 2009 Feb 17;8:3. doi: 10.1186/1477-5751-8-3.
Ye YL, Shi WZ, Zhang WP, Wang ML, Zhou Y, Fang SH, Liu LY, Zhang Q, Yu YP, Wei EQ. Cilostazol, a phosphodiesterase 3 inhibitor, protects mice against acute and late ischemic brain injuries. Eur J Pharmacol. 2007 Feb 14;557(1):23-31. doi: 10.1016/j.ejphar.2006.11.003. Epub 2006 Nov 10.
Related Links
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Clinical Research Information Service (CRIS)
Institutional Review Board of Asan Medical Center
Other Identifiers
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KCT0000128
Identifier Type: REGISTRY
Identifier Source: secondary_id
AMC-2010-0800
Identifier Type: -
Identifier Source: org_study_id
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