UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000060190 |
|---|---|
| Receipt number | R000068689 |
| Scientific Title | Cross-sectional study of aging-related indicators |
| Date of disclosure of the study information | 2025/12/26 |
| Last modified on | 2025/12/24 13:07:42 |
* 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
Cross-sectional study of aging-related indicators
Acronym
Cross-sectional study of aging-related indicators
Scientific Title
Cross-sectional study of aging-related indicators
Scientific Title:Acronym
Cross-sectional study of aging-related indicators
Region
| Japan |
Condition
Condition
Healthy adults
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
YES
Objectives
Narrative objectives1
To examine associations of aging-related biological indicators with clinical, questionnaire, and imaging findings.
Basic objectives2
Others
Basic objectives -Others
To examine associations of aging-related biological indicators with clinical, questionnaire, and imaging findings.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Associations among biological indicators, physical examination findings, questionnaire results, imaging analyses, and participant characteristics
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
| 70 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Japanese participants aged 20 to 69 years at the time of consent.
Key exclusion criteria
1) Participants with a history of severe diseases and a history of gastrointestinal resection surgery (excluding appendectomy).
2) Participants with heavy alcohol consumption and excessive smoking.
3) Participants whose examination day falls during menstruation.
4) Pregnant participants.
5) Participants with an implanted cardiac pacemaker.
6) Participants judged inappropriate for participation by the principal investigator.
Target sample size
200
Research contact person
Name of lead principal investigator
| 1st name | Tamie |
| Middle name | |
| Last name | Suzuki |
Organization
FANCL Corporation
Division name
Research Institute
Zip code
244-0806
Address
12-13, Kamishinano, Totsuka-ku, Yokohama, Kanagawa, Japan
TEL
045-820-3857
tamisuzuki@fancl.co.jp
Public contact
Name of contact person
| 1st name | Naoyuki |
| Middle name | |
| Last name | Abe |
Organization
Medical Corporation Jikokai Shiroishi Internal Medicine Clinic
Division name
Clinical Trial Division
Zip code
003-0011
Address
7-10-30 Chuo-1 jo, Shiroishi-ku, Sapporo, Hokkaido, Japan
TEL
011-868-2711
Homepage URL
n-abe@medi-ate.jp
Sponsor or person
Institute
FANCL Corporation
Institute
Department
Personal name
Funding Source
Organization
FANCL Corporation
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
Medical Corporation Jikokai Fukuzumi Internal Medicine Clinic Institutional Review Board
Address
1-2-5 Fukuzumi-2 jo, Toyohira-ku, Sapporo, Hokkaido, Japan
Tel
011-836-3531
n-abe@medi-ate.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
医療法人社団慈昂会 白石内科クリニック
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 12 | Month | 26 | 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
| 2025 | Year | 12 | Month | 08 | Day |
Date of IRB
| 2025 | Year | 12 | Month | 19 | Day |
Anticipated trial start date
| 2026 | Year | 02 | Month | 02 | Day |
Last follow-up date
| 2026 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
The purpose of this study is to investigate the association of aging-related biomarkers, physical examination findings, questionnaire responses, and image analysis results with aging.
Management information
Registered date
| 2025 | Year | 12 | Month | 24 | Day |
Last modified on
| 2025 | Year | 12 | Month | 24 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068689
