A Study on the Effect of Cilostazol in Patients With Chronic Tinnitus

NCT ID: NCT01378650

Last Updated: 2014-05-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-07-31

Study Completion Date

2013-06-30

Brief Summary

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1. Overview of tinnitus Tinnitus is a noisy sound which is perceived without any external sound source. According to the survey of the US, 10-20% of adult have the symptom of tinnitus and 3-5% of tinnitus patients have severe discomfort of daily life. Severe tinnitus can result in psychiatric problems such as depression and anxiety disorders. Enhancement of environmental sound, hearing aids, sound generators, cognitive therapy, transcranial magnetic therapy, and drug therapy have been tried for treatment of tinnitus. Nitric oxide(NO) is a well-known neurotransmitter acting as a vasodilator through regulation of production of cyclic guanosine monophosphate(cGMP) and can be found in various sites of cochlea. It is reported that cGMP enhances activity of protein kinase A (PKA), a mediator of platelet aggregation inhibition and vasodilatation and results in increase of vascular flow.
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.

Detailed Description

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1. Clinical research methods

* 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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Tinnitus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Cilostazol group

Administration of Cilostazol 100mg twice a day for 4 weeks

Group Type EXPERIMENTAL

Cilostazol

Intervention Type DRUG

Administration of Cilostazol 100mg twice a day for 4 weeks

Placebo group

placebo drug twice a day for 4 weeks.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

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

Intervention Type DRUG

Placebo

placebo one tablet matching for cilostazol twice a day for 4 weeks.

Intervention Type DRUG

Other Intervention Names

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Pletaal Placebo matching for cilostazol

Eligibility Criteria

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Inclusion Criteria

* Adults of age over 19
* Unilateral or bilateral tinnitus
* Chronic tinnitus lasting more than 3 months
* Initial visual analogue scale of tinnitus \>3

Exclusion Criteria

* Conductive hearing loss on pure tone audiometry
* 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
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Korea Otsuka Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role collaborator

Jong Woo Chung

OTHER

Sponsor Role lead

Responsible Party

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Jong Woo Chung

MD

Responsibility Role SPONSOR_INVESTIGATOR

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

Site Status

Countries

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South Korea

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.

Reference Type BACKGROUND
PMID: 19222841 (View on PubMed)

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.

Reference Type BACKGROUND
PMID: 17161838 (View on PubMed)

Related Links

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https://cris.nih.go.kr/cris/index.jsp

Clinical Research Information Service (CRIS)

http://crc.amc.seoul.kr

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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