UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000000672
Receipt number R000000808
Scientific Title Prediction of drug adverse event through gene expression analysis
Date of disclosure of the study information 2007/04/05
Last modified on 2012/04/09 15:42:02

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Basic information

Public title

Prediction of drug adverse event through gene expression analysis

Acronym

Prediction of drug adverse event through gene expression analysis

Scientific Title

Prediction of drug adverse event through gene expression analysis

Scientific Title:Acronym

Prediction of drug adverse event through gene expression analysis

Region

Japan


Condition

Condition

embedded dens molaris

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to confirm gene expression related to drug adverse events

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

correlation and differences of gene expression between results from basic experiments in vitro and ones in human

Key secondary outcomes



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

Cefcapene Pivoxil Hydrochloride Hydrate 100mg po administration for three times

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

60 years-old >=

Gender

Male and Female

Key inclusion criteria

those who are planned to receive exodontics of one of embedded third dens molaris

Key exclusion criteria

renal dysfunction (Creatinin equal or greater than 2.0 mg/dl)
liver dysfunction (ALT, AST, T-bil, LDH or ALP are more than two times greater than upper limit of normal range)
confirmed or clinically suspected myocardial infarction and/or congestive heart failure
prescribed medicines for diabetes mellitus and/or hypertension
pasthistory for hypersensitivities and/or allargic reactions against Cefcapene Pivoxil Hydrochloride Hydrate or ingredients of Flomox(R)
Past history of hypersensitivities for Cephalosporins

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Akio Fujimura, MD, PhD

Organization

Jichi Medical University

Division name

Clinical Pharmacology

Zip code


Address

Shimotsuke-si, Tochigi-ken

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Jichi Medical University

Division name

SCHOOL AFFAIRS SECTION

Zip code


Address


TEL

0285-58-7550

Homepage URL


Email



Sponsor or person

Institute

JICHI MEDICAL UNIVERSITY

Institute

Department

Personal name



Funding Source

Organization

HEALTH AND LABOUR SCIENCES RESEARCH GRNTS

Organization

Division

Category of Funding Organization

Nationality of Funding Organization



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

2007 Year 04 Month 05 Day


Related information

URL releasing protocol


Publication of results

Unpublished


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

2006 Year 12 Month 18 Day

Date of IRB


Anticipated trial start date

2007 Year 01 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete

2008 Year 03 Month 01 Day

Date analysis concluded

2009 Year 03 Month 01 Day


Other

Other related information



Management information

Registered date

2007 Year 04 Month 05 Day

Last modified on

2012 Year 04 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000808


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name