UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000063623 |
|---|---|
| Receipt number | R000072816 |
| Scientific Title | An Exploratory Study on Factors Correlated with Blood Plastic Concentration |
| Date of disclosure of the study information | 2026/11/13 |
| Last modified on | 2026/11/13 15:44:24 |
* 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
An Exploratory Study on Factors Correlated with Blood Plastic Concentration
Acronym
An Exploratory Study on Factors Correlated with Blood Plastic Concentration
Scientific Title
An Exploratory Study on Factors Correlated with Blood Plastic Concentration
Scientific Title:Acronym
An Exploratory Study on Factors Correlated with Blood Plastic Concentration
Region
| Japan |
Condition
Condition
Adults
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Exploring factors correlated with blood plastic concentration
Basic objectives2
Others
Basic objectives -Others
Exploring factors correlated with blood plastic concentration
Trial characteristics_1
Exploratory
Trial characteristics_2
Developmental phase
Not applicable
Assessment
Primary outcomes
Analyze the correlation between age and blood plastic concentration.
Analyze the correlation between intestinal barrier function markers and blood plastic concentration.
Key secondary outcomes
Base
Study type
Observational
Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
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
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1. Male and female who were in their 20s or aged 60 and over at the time of consent acquisition.
2. Subjects who provide written informed consent.
Key exclusion criteria
1. Subjects who have donated blood within the past month.
2. Subjects who have undergone or may have undergone any of the following procedures within the past year: intravenous drip, blood transfusion, administration of blood products, component blood donation, surgery (excluding upper and lower endoscopic biopsies), hemodialysis, apheresis, use of an intravenous catheter, or intravenous injection.
3. Subjects who currently have an indwelling intravascular device.
4. Subjects with a known metal allergy.
5. Subjects with a self-reported or known infection of viral hepatitis (Type B or C), HIV, or syphilis, or who have tested positive for an infectious disease via a screening test.
6. Subjects deemed unsuitable for blood collection by the phlebotomist/staff.
7. Subjects deemed unsuitable by the investigator.
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | Shukuko |
| Middle name | |
| Last name | Ebihara |
Organization
Chiyoda Paramedical Care Clinic
Division name
Clinic Director
Zip code
103-0021
Address
2F Daiwa Building, 3-3-10 Nihonbashi-Hongoku-Cho, Chuo-ku, Tokyo 103-0021, Japan
TEL
03-6225-9005
cpcc-contact@cpcc.co.jp
Public contact
Name of contact person
| 1st name | Shingo |
| Middle name | |
| Last name | Tsukamoto |
Organization
CPCC Company Limited
Division name
Clinical Planning Department
Zip code
103-0021
Address
4F Daiwa Building, 3-3-10 Nihonbashi-Hongoku-Cho, Chuo-ku, Tokyo, Japan
TEL
03-6225-9001
Homepage URL
cpcc-contact@cpcc.co.jp
Sponsor or person
Institute
Meiji Co., Ltd.
Institute
Department
Personal name
Funding Source
Organization
Meiji Co., Ltd
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Institutional Review Board of Chiyoda Paramedical Care Clinic
Address
2F Daiwa Building, 3-3-10 Nihonbashi-Hongoku-Cho, Chuo-ku, Tokyo 103-0021, Japan
Tel
03-6225-9005
IRB@cpcc.co.jp
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
チヨダパラメディカルケアクリニック（東京都）
Chiyoda Paramedical Care Clinic (Tokyo)
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 11 | Month | 13 | 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
Preinitiation
Date of protocol fixation
| 2026 | Year | 09 | Month | 29 | Day |
Date of IRB
| 2026 | Year | 09 | Month | 18 | Day |
Anticipated trial start date
| 2026 | Year | 11 | Month | 19 | Day |
Last follow-up date
| 2026 | Year | 12 | Month | 14 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
analysis of blood plastic concentration
Management information
Registered date
| 2026 | Year | 11 | Month | 13 | Day |
Last modified on
| 2026 | Year | 11 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072816
