UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000005838
Receipt number R000006841
Scientific Title Assessment of cell proliferation using FLT-PET for FDG-avid parotid tumor
Date of disclosure of the study information 2011/07/01
Last modified on 2016/08/24 09:13:06

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Basic information

Public title

Assessment of cell proliferation using FLT-PET for FDG-avid parotid tumor

Acronym

FLT-PET for FDG-avid parotid tumor

Scientific Title

Assessment of cell proliferation using FLT-PET for FDG-avid parotid tumor

Scientific Title:Acronym

FLT-PET for FDG-avid parotid tumor

Region

Japan


Condition

Condition

Parotid tumor

Classification by specialty

Oto-rhino-laryngology Radiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the clinical value of FLT-PET for the patients with FDG-avid parotid tumor

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Correlation between FLT uptake and clinical diagnosis / FDG uptake

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Medicine Device,equipment

Interventions/Control_1

FLT-PET

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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. FDG-PET was performed within 2 months before entering this study
2. FDG-avid parotid tumor was pointed out, and examined at otorhinolaryngology department of KCMCGH
3. Diameter of the parotid tumor was 1cm or more confirmed by CT / MRI / US
4. Patients understood well their condition of the disease

Key exclusion criteria

1. Poor general condition
2. Cannot keep supine position for 60 minutes
3. Pregnant or possibility of pregnancy
4. Severe claustrophobia
5. Regarded as unsuitable by responsible investigators

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Michio Senda

Organization

Institute of Biomedical Research and Innovation

Division name

Division of Molecular Imaging

Zip code


Address

2-2, Minatojima-Minamimachi, Chuo-Ku, Kobe

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Institute of Biomedical Research and Innovation

Division name

Division of Molecular Imaging

Zip code


Address

2-2, Minatojima-Minamimachi, Chuo-Ku, Kobe

TEL

078-306-1700

Homepage URL


Email



Sponsor or person

Institute

Foundation of Biomedical Research and Innovation

Institute

Department

Personal name



Funding Source

Organization

Foundation of Biomedical Research and Innovation

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization

Japan


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

2011 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

Terminated

Date of protocol fixation

2011 Year 06 Month 15 Day

Date of IRB


Anticipated trial start date

2011 Year 07 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2011 Year 06 Month 23 Day

Last modified on

2016 Year 08 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006841


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name