UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022828
Receipt number R000026306
Scientific Title Long-term outcomes after carbon ion radiotherapy for oral mucosal malignant melanoma
Date of disclosure of the study information 2016/07/01
Last modified on 2019/01/18 21:40:54

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Basic information

Public title

Long-term outcomes after carbon ion radiotherapy for oral mucosal malignant melanoma

Acronym

Long-term outcomes after carbon ion radiotherapy for oral mucosal malignant melanoma

Scientific Title

Long-term outcomes after carbon ion radiotherapy for oral mucosal malignant melanoma

Scientific Title:Acronym

Long-term outcomes after carbon ion radiotherapy for oral mucosal malignant melanoma

Region

Japan


Condition

Condition

Mucosal malignant melanoma

Classification by specialty

Radiology Dental medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

This study is to evaluate the long-term efficacy of carbon-ion radiotherapy (C-ion RT) for Oral mucosal malignant melanoma.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

5-year overall survival rate

Key secondary outcomes

5-year local control rate, Toxicities (acute and late)


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

patients treated with C-ion RT alone.
All tumors were pathologically confirmed.
The patients had medically inoperable tumors or declined surgery.

Key exclusion criteria

All patients received C-ion RT as the primary treatment.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Koto Masashi

Organization

National Institute of Radiological Science Hospital, National Institutes for Quantum and Radiological Sciences and Technology

Division name

National Institute of Radiological Science Hospital

Zip code


Address

Anagawa 4-9-1, Inage-ku 263-8555 Chiba, Japan

TEL

043-206-3360

Email

koto.masashi@qst.go.jp


Public contact

Name of contact person

1st name
Middle name
Last name Koto Masashi

Organization

National Institutes for Quantum and Radiological Sciences and Technology

Division name

National Institute of Radiological Science Hospital

Zip code


Address

Anagawa 4-9-1, Inage-ku 263-8555 Chiba, Japan

TEL

043-206-3360

Homepage URL


Email

koto.masashi@qst.go.jp


Sponsor or person

Institute

The Research Project with Heavy Ions at the National Institute of radiological Sciences (NIRS)-Heavy Ion Medical Accelerator in Chiba (HIMAC).

Institute

Department

Personal name



Funding Source

Organization

none

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


Address


Tel


Email



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

2016 Year 07 Month 01 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

Completed

Date of protocol fixation

2016 Year 06 Month 21 Day

Date of IRB


Anticipated trial start date

2016 Year 06 Month 22 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Retrospective study


Management information

Registered date

2016 Year 06 Month 21 Day

Last modified on

2019 Year 01 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026306