UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Terminated
Unique ID issued by UMIN UMIN000002662
Receipt No. R000003234
Scientific Title Interindividual variation of perception threshold -Examination with Neurometer®
Date of disclosure of the study information 2009/10/23
Last modified on 2010/10/23

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title Interindividual variation of perception threshold -Examination with Neurometer®
Acronym Interindividual variation of perception threshold
Scientific Title Interindividual variation of perception threshold -Examination with Neurometer®
Scientific Title:Acronym Interindividual variation of perception threshold
Region
Japan

Condition
Condition pain
Classification by specialty
Medicine in general Hematology and clinical oncology Psychosomatic Internal Medicine
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To investigate the distribution of perception threshold about young, healthy Japanese, and to examine the effect of NSAID to percption threshold.
Basic objectives2 Pharmacodynamics
Basic objectives -Others
Trial characteristics_1 Exploratory
Trial characteristics_2
Developmental phase Not applicable

Assessment
Primary outcomes CPT value
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 Loxoprofen oral dosing
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
40 years-old >
Gender Male and Female
Key inclusion criteria healthy, young Japanese
Key exclusion criteria recent participation to other clinical trial
history of any drug allergy
Target sample size 20

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Dr. Hiromitsu Imai
Organization Oita university, Faculty of medicine
Division name Dept of clinical pharmacology and therapeutics
Zip code
Address 1-1 Idaigaoka Hasama Yufu-city, Oita, JAPAN
TEL
Email

Public contact
Name of contact person
1st name
Middle name
Last name Dr. Hiromitsu Imai
Organization Oita university, Faculty of medicine
Division name Dept of clinical pharmacology
Zip code
Address 1-1 Idaigaoka Hasama Yufu-city, Oita, JAPAN
TEL
Homepage URL
Email

Sponsor
Institute Dept of clinical pharmacology and therapeutics, Oita university, Faculty of medicine
Institute
Department

Funding Source
Organization Dept of clinical pharmacology and therapeutics, Oita university, Faculty of medicine
Organization
Division
Category of Funding Organization Self funding
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
2009 Year 10 Month 23 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 Terminated
Date of protocol fixation
2009 Year 09 Month 08 Day
Date of IRB
Anticipated trial start date
2009 Year 10 Month 01 Day
Last follow-up date
2010 Year 03 Month 01 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information

Management information
Registered date
2009 Year 10 Month 23 Day
Last modified on
2010 Year 10 Month 23 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003234

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.