| Recruitment status | Preinitiation |
| Unique ID issued by UMIN | UMIN000022033 |
| Receipt No. | R000025398 |
| Official scientific title of the study | Epidemiological studies of the incidence and mortality in after the end of the period of Neuroblastoma screening |
| Date of disclosure of the study information | 2016/05/05 |
| Last modified on | 2016/04/23 (Ver. 1) |
| Basic information | ||
| Official scientific title of the study | Epidemiological studies of the incidence and mortality in after the end of the period of Neuroblastoma screening | |
| Title of the study (Brief title) | Epidemiological studies after the end of the period of Neuroblastoma screening | |
| Region |
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| Condition | |||
| Condition | neuroblastoma | ||
| Classification by specialty |
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| Classification by malignancy | Malignancy | ||
| Genomic information | NO | ||
| Objectives | |
| Narrative objectives1 | The purpose of this study is to clarify the incidence and mortality of neuroblastoma before and after the end of infancy neuroblastoma screening. |
| Basic objectives2 | Others |
| Basic objectives -Others | The purpose is to analyze the changes in morbidity and mortality in a cohort of the the before and after the end of the period of Neuroblastoma screening |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | incidence and mortality rate |
| Key secondary outcomes | |
| In outcomes field, the entry of just a few words such as "safety" or "efficiency" will not be accepted. Specify the name of outcome measures, including the time when you plan to measure. Usually, only one primary outcome is accepted. Write the other outcomes in "secondary outcomes" field. |
| 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 | |
| In interventions field, include the details of interventions, such as duration, amount, and frequency. If the intervention includes prescription or use of medical devices, duration is required. |
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | neuroblastoma | |||
| Key exclusion criteria | none | |||
| Target sample size | 800 | |||
| Research contact person | |
| Name of lead principal investigator | Tomoko Iehara |
| Organization | Kyoto Prefectural University of Medicine |
| Division name | Pediatrics |
| Address | Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JAPAN |
| TEL | 0752515111 |
| iehara@koto.kpu-m.ac.jp | |
| Public contact | |
| Name of contact person | Tomoko Iehara |
| Organization | Kyoto Prefectural University of Medicine |
| Division name | Pediatrics |
| Address | Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JAPAN |
| TEL | 0752515111 |
| Homepage URL | |
| iehara@koto.kpu-m.ac.jp | |
| Sponsor | |
| Institute | Kyoto Prefectural University of Medicine |
| Institute | |
| Department | |
| Sponsor means an organization that is responsible for plan, deployment and report of the research including funding management. It doesn't mean funding agency". Therefore, all clinical trial should have the one. |
| Funding Source | |
| Organization | Ministry of Health, Labour and Welfare |
| Organization | |
| Division | |
| Category of Funding Organization | Japanese Governmental office |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| 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 | |
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| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Preinitiation | ||||||
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| Anticipated trial start date |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| URL releasing results | |
| Results | |
| Other related information | Health and Labor Sciences Research Grant |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025398 |