UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000004542
Receipt number R000005428
Scientific Title Clinical study of gatiflixacin on male non-gonococcal urethritis
Date of disclosure of the study information 2010/11/11
Last modified on 2010/11/11 13:28:33

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Basic information

Public title

Clinical study of gatiflixacin on male non-gonococcal urethritis

Acronym

GONG study

Scientific Title

Clinical study of gatiflixacin on male non-gonococcal urethritis

Scientific Title:Acronym

GONG study

Region

Japan


Condition

Condition

Non-gonococcal urethritis

Classification by specialty

Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the microbiological or clinical efficacies of garifloxacin against male non-gonococcal urethritis

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Phase IV


Assessment

Primary outcomes

To evaluate the microbiological efficacies of gatifloxacin against microorganisms of non-gonococcal urethritis
To examine the antimicrobial susceptibilitities of Mycoplasma genitalium to fluoroquinolones

Key secondary outcomes

To evaluate the clinical efficacies of gatifloxacin to non-gonococcal urethritis


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Gatifloxacin with 200mg is administrated twice a day for 7 days

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

65 years-old >=

Gender

Male

Key inclusion criteria

Male patient with non-gonococcal urethritis

Key exclusion criteria

Patients with gonococcal urethritis Patients who have sexual intercourse without using condom

Target sample size

300


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Ryoichi Hamasuna

Organization

University of Occupational and Environmental Health

Division name

Department of Urology

Zip code


Address

1-1,Iseigaoka,Yahata-nishi-ku,kitakyushu,fukuoka,807-8555,Japan

TEL

093-691-7446

Email



Public contact

Name of contact person

1st name
Middle name
Last name Ryoichi Hamasuna

Organization

University of Occupational and Environmental Health

Division name

Department of Urology

Zip code


Address

1-1,Iseigaoka,Yahata-nishi-ku,kitakyushu,fukuoka,807-8555 Japan

TEL

093-691-7446

Homepage URL


Email

hamaryo@med.uoeh-u.ac.jp


Sponsor or person

Institute

NPO CREC net

Institute

Department

Personal name



Funding Source

Organization

Non

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2010 Year 11 Month 11 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2007 Year 12 Month 20 Day

Date of IRB


Anticipated trial start date

2008 Year 04 Month 01 Day

Last follow-up date

2009 Year 03 Month 01 Day

Date of closure to data entry

2009 Year 05 Month 01 Day

Date trial data considered complete

2009 Year 05 Month 01 Day

Date analysis concluded

2009 Year 05 Month 01 Day


Other

Other related information



Management information

Registered date

2010 Year 11 Month 11 Day

Last modified on

2010 Year 11 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005428


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name