| Recruitment status | Enrolling by invitation |
| Unique ID issued by UMIN | UMIN000029320 |
| Receipt No. | R000033497 |
| Official scientific title of the study | Immune function analysis after sirolimus treatment for pediatric patients with intractable vascular anomalies |
| Date of disclosure of the study information | 2017/09/29 |
| Last modified on | 2017/09/27 (Ver. 1) |
| Basic information | ||
| Official scientific title of the study | Immune function analysis after sirolimus treatment for pediatric patients with intractable vascular anomalies | |
| Title of the study (Brief title) | Immune function analysis after sirolimus treatment for pediatric patients with intractable vascular anomalies | |
| Region |
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| Condition | |||||||||||||||||||
| Condition | Intractable vascular anomalies | ||||||||||||||||||
| Classification by specialty |
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| Classification by malignancy | Others | ||||||||||||||||||
| Genomic information | NO | ||||||||||||||||||
| Objectives | |
| Narrative objectives1 | To investigate immune function analysis after sirolimus treatment for the Japanese pediatric patients |
| Basic objectives2 | Others |
| Basic objectives -Others | To research the association between the sirolimus treatment and infection frequency |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | Immune function analysis after sirolimus treatment for the Japanese pediatric patients |
| Key secondary outcomes | The association between the sirolimus treatment and infection frequency |
| 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 | Intractable vascular anomalies | |||
| Key exclusion criteria | 1. Patients with a history of hypersensitivity to ingredients of this drug
2. Patients with serious liver and renal disorders 3. Patients with symptoms that affect cytokine value of such obvious infection at the time of specimen collection 4. Patients must also avoid strong inducers of CYP3A4 5. Past usage of mTOR inhibitors or other molecular target drugs relating mTOR pathway 6. Patient who is judged inappropriate to participate in this study by the investigators |
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| Target sample size | 10 | |||
| Research contact person | |
| Name of lead principal investigator | Michio Ozeki |
| Organization | Gifu University Hospital |
| Division name | The department of Pediatrics |
| Address | 1-1 Yanagito, Gifu-shi, Gifu-ken |
| TEL | 058-230-6000 |
| michioo@gifu-u.ac.jp | |
| Public contact | |
| Name of contact person | Michio Ozeki |
| Organization | Gifu University Hospital |
| Division name | The department of Pediatrics |
| Address | 1-1 Yanagito, Gifu-shi, Gifu-ken |
| TEL | 058-230-6000 |
| Homepage URL | |
| michioo@gifu-u.ac.jp | |
| Sponsor | |
| Institute | Gifu University |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Japan Agency for Medical Research and Development |
| 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 | |
| Institutions | (国立成育医療研究センター(東京都)、慶應義塾大学病院(東京都)、京都府立医科大学附属病院(京都)、九州大学病院(福岡県)、浜松医科大学(静岡県) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Enrolling by invitation | ||||||
| Date of protocol fixation |
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| Anticipated trial start date |
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| Last follow-up date | |||||||
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| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| URL releasing results | |
| Results | |
| Other related information | For more information, please contact the Principal Investigator. |
| 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=R000033497 |