| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000012978 |
| Receipt No. | R000015126 |
| Official scientific title of the study | Clinical study of microRNA analysis of serum in Pediatric inflammatory disease |
| Date of disclosure of the study information | 2014/02/06 |
| Last modified on | 2016/08/09 (Ver. 11) |
| Basic information | ||
| Official scientific title of the study | Clinical study of microRNA analysis of serum in Pediatric inflammatory disease | |
| Title of the study (Brief title) | Clinical study of microRNA analysis of serum in Pediatric inflammatory disease | |
| Region |
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| Condition | |||
| Condition | Pediatric inflammatory disease | ||
| Classification by specialty |
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| Classification by malignancy | Others | ||
| Genomic information | NO | ||
| Objectives | |
| Narrative objectives1 | Objectives of this study are
1. to search biomarkers reflecting disease state 2. to search biomarkers to predict severity and response to treatment in patients of pediatric inflammatory diseases patients including JIA(Juvenile idiopathic arthritis). |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | Measurement of microRNA in serum samples of patients |
| 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 |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | who consent to participate in this study, of patients who were diagnosed with pediatric inflammatory diseases in pediatric Clinical facility | |||
| Key exclusion criteria | Not obtained the consent | |||
| Target sample size | 30 | |||
| Research contact person | |
| Name of lead principal investigator | Ken Ishii |
| Organization | National Institutes of Biomedical Innovation,Health and Nutrition |
| Division name | Laboratory of Adjuvant Innovation |
| Address | 7-6-8 Asagi Saito Ibaraki-City Osaka |
| TEL | 072-641-8043 |
| kenishii@biken.osaka-u.ac.jp | |
| Public contact | |
| Name of contact person | Ken Ishii |
| Organization | National Institutes of Biomedical Innovation,Health and Nutrition |
| Division name | Laboratory of Adjuvant Innovation |
| Address | 7-6-8 Asagi Saito Ibaraki-City Osaka |
| TEL | 072-641-8043 |
| Homepage URL | |
| kenishii@biken.osaka-u.ac.jp | |
| Sponsor | |
| Institute | National Institutes of Biomedical Innovation,Health and Nutrition |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Japan Agency for Medical Research and Development |
| Organization | |
| Division | |
| Category of Funding Organization | Other |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | Yokohama City University Hospital of Pediatrics |
| Name of secondary funder(s) | |
| 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 |
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| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
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| Anticipated trial start date |
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| Last follow-up date | |||||||
| Date of closure to data entry | |||||||
| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| URL releasing results | |
| Results | |
| Other related information | About sumple
Serum(about 0.5 to 1.0ml) of acute phase and remisson phase are collected from subjects in Clinical facility of this study. Then samples are only numbered and transported to National Institute of Biomedical Innovation. |
| Management information | |||||||
| Registered date |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000015126 |