UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020138
Receipt number R000023093
Scientific Title Study on 11C-ITMM accumlation in epileptic foci
Date of disclosure of the study information 2015/12/10
Last modified on 2019/12/12 19:21:10

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Basic information

Public title

Study on 11C-ITMM accumlation in epileptic foci

Acronym

11C-ITMM PET in epilepsy

Scientific Title

Study on 11C-ITMM accumlation in epileptic foci

Scientific Title:Acronym

11C-ITMM PET in epilepsy

Region

Japan


Condition

Condition

partial epilepsy

Classification by specialty

Neurology Radiology Neurosurgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluation on accumulation of C-11 ITMM in epileptic foci

Basic objectives2

Pharmacokinetics

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Explanatory

Developmental phase

Phase II


Assessment

Primary outcomes

Distribution of C-11 ITMM in epileptic foci
Date of evaluation: on the day of PET scan

Key secondary outcomes

Distribution of C-11 flumazenil in epileptic foci
Date of evaluation: on the day of PET scan


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Medicine

Interventions/Control_1

The dosage in the vain of [C-11]ITMM for PET/CT imaging.

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

60 years-old >=

Gender

Male and Female

Key inclusion criteria

1. Patients diagnosed as having epilepsy.
2. Parients being suspected of partial seizure based on seizure symptoms, brain MRI and FDG-PET findings.
3. Patients with documented agreement on the informed consent by themselves or by their legally acceptable representatives.

Key exclusion criteria

1. Patients who are suspected of generalized seizure.
2. Patients accompanied by chronic renal failure.
3. Pregnant women or possible pregnant women.
4. The patient who judged by the clinical investigator to be inappropriate as a participant in this study.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Kenji
Middle name
Last name Ishii

Organization

Tokoyo Metropolitan Institute of Gerontology

Division name

Research Team for Neuroimaging

Zip code

173-0015

Address

35-2 Sakae-cho, Itabashi-ku, Tokyo

TEL

03-3964-3241

Email

ishii@pet.tmig.or.jp


Public contact

Name of contact person

1st name Kenji
Middle name
Last name Ishii

Organization

Tokyo Metropolitan Institute of Gerontology

Division name

Research Team for Neuroimaging

Zip code

173-0015

Address

Itabashi-ku

TEL

03-3964-3241

Homepage URL


Email

ishii@pet.tmig.or.jp


Sponsor or person

Institute

Tokoyo Metropolitan Institute of Gerontology

Institute

Department

Personal name



Funding Source

Organization

Tokoyo Metropolitan Institute of Gerontology

Organization

Division

Category of Funding Organization

Local Government

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Committee, Tokyo Metropolitan Institute of Gerontology

Address

35-2 Sakaecyo, Itabashi-ku, Tokyo, Japan

Tel

03-3964-3241

Email

naomi_hasegawa@tmghig.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

地方独立行政法人東京都健康長寿医療センター研究所


Other administrative information

Date of disclosure of the study information

2015 Year 12 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

Completed

Date of protocol fixation

2015 Year 10 Month 14 Day

Date of IRB

2017 Year 06 Month 25 Day

Anticipated trial start date

2015 Year 12 Month 21 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 12 Month 09 Day

Last modified on

2019 Year 12 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023093


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name