UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000061860 |
|---|---|
| Receipt number | R000070785 |
| Scientific Title | Observational study on the correlation between blood ferritin concentration and urinary ferritin concentration |
| Date of disclosure of the study information | 2026/06/10 |
| Last modified on | 2026/06/10 18:16:08 |
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Basic information
Public title
Observational study on the correlation between blood ferritin concentration and urinary ferritin concentration
Acronym
Observational study on the correlation between blood ferritin concentration and urinary ferritin concentration
Scientific Title
Observational study on the correlation between blood ferritin concentration and urinary ferritin concentration
Scientific Title:Acronym
Observational study on the correlation between blood ferritin concentration and urinary ferritin concentration
Region
| Japan |
Condition
Condition
Healthy Adults
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the correlation between blood ferritin concentration and urinary ferritin concentration.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Blood ferritin concentration Urinary ferritin 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
| 18 | years-old | <= |
Age-upper limit
| 65 | years-old | > |
Gender
Male and Female
Key inclusion criteria
1. Persons who received a sufficient explanation of the purpose and contents of the study, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate.
2. Japanese who are 18 years old or more and under 65 years old at the time of consent.
Key exclusion criteria
1. Persons who have chronic illness, receiving medication, have a serious disease history (including patients with inflammatory diseases (such as inflammatory bowel disease (IBD), chronic heart failure (CHF), chronic kidney disease (CKD)), liver disease, various cancers, hemolytic anemia, and muscular dystrophy).
2. Persons who have participated in other studies within one month before the start of the study, or those who intend to participate in another study after consenting to this study.
3. Persons who were judged as inappropriate for study participants by the principal investigator or the lead principal investigator.
Target sample size
50
Research contact person
Name of lead principal investigator
| 1st name | Masashi |
| Middle name | |
| Last name | Nagai |
Organization
Healthcare Systems Co., Ltd.
Division name
Research and Development Department
Zip code
466-0058
Address
1-14-18, Shirakane, Showa-ku, Nagoya, Aichi, JAPAN
TEL
03-6809-2722
nagai@hc-sys.jp
Public contact
Name of contact person
| 1st name | Takamasa |
| Middle name | |
| Last name | Masuda |
Organization
Healthcare Systems Co., Ltd.
Division name
Clinical Research Department
Zip code
105-0004
Address
Park Place Bld. 5F, 5-27-1, Shinbashi, Minato-ku, Tokyo, JAPAN
TEL
03-6809-2722
Homepage URL
masudat@hc-sys.jp
Sponsor or person
Institute
Healthcare Systems Co., Ltd.
Institute
Department
Personal name
Funding Source
Organization
self funding
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
The Ethics Committee of Healthcare Systems Co., Ltd.
Address
1-14-18, Shirakane, Showa-ku, Nagoya, Aichi, JAPAN
Tel
03-6809-2722
soumu@hc-sys.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
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 06 | Month | 10 | 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 | 04 | Month | 30 | Day |
Date of IRB
| 2026 | Year | 05 | Month | 07 | Day |
Anticipated trial start date
| 2026 | Year | 07 | Month | 08 | Day |
Last follow-up date
| 2026 | Year | 10 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Analysis of the correlation between blood ferritin concentration and urinary ferritin concentration in Japanese men and women.
Management information
Registered date
| 2026 | Year | 06 | Month | 10 | Day |
Last modified on
| 2026 | Year | 06 | Month | 10 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000070785
