UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000025563 |
|---|---|
| Receipt number | R000028701 |
| Scientific Title | Exploratory study to estimate blood parameter by sensor. |
| Date of disclosure of the study information | 2017/01/07 |
| Last modified on | 2017/05/10 21:33:45 |
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Basic information
Public title
Exploratory study to estimate blood parameter by sensor.
Acronym
Exploratory study to estimate blood parameter by sensor.
Scientific Title
Exploratory study to estimate blood parameter by sensor.
Scientific Title:Acronym
Exploratory study to estimate blood parameter by sensor.
Region
| Japan |
Condition
Condition
Not applicable
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the correlation between amounts of sensor measurement and blood parameter.
Basic objectives2
Others
Basic objectives -Others
Method of measurement.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Correlation between amounts of sensor measurement and blood parameter.
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
Prevention
Type of intervention
| Device,equipment |
Interventions/Control_1
Wearing of the optical sensor for 3 hours.
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
(1) BMI less than 30.
(2)Subjects who are able to submit the written informed consents.
Key exclusion criteria
(1)Subjects who are with treatment.
(2)Females in pregnancy, lactation and scheduled pregnancy period.
(3)Subjects who are;
(a)With present heart disorder, liver disorder, or kidney disorder,
(b)With history of cardiac disorder,
(c)With diabetes mellitus, or
(5)Subjects who habitually intake drugs.
(6)Subjects who experienced unpleasant feeling during drawing blood.
(7)Subjects who are deemed to be unsuitable by the investigator.
Target sample size
70
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Mitsuhiro Zeida |
Organization
Suntory Global Innovation Center Limited
Division name
Research Institute
Zip code
Address
8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto, Japan
TEL
050-3182-0464
Mitsuhiro_Zeida@suntory.co.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Mitsuhiro Zeida |
Organization
Suntory Global Innovation Center Limited
Division name
Research Institute
Zip code
Address
8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto, Japan
TEL
050-3182-0464
Homepage URL
Mitsuhiro_Zeida@suntory.co.jp
Sponsor or person
Institute
Suntory Global Innovation Center Limited
Institute
Department
Personal name
Funding Source
Organization
Suntory Global Innovation Center Limited
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
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
小鮒整形外科医院
Other administrative information
Date of disclosure of the study information
| 2017 | Year | 01 | Month | 07 | 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
| 2016 | Year | 11 | Month | 17 | Day |
Date of IRB
Anticipated trial start date
| 2016 | Year | 12 | Month | 03 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2017 | Year | 01 | Month | 06 | Day |
Last modified on
| 2017 | Year | 05 | Month | 10 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028701
