UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029750
Receipt number R000033989
Scientific Title Diagnosis of prostate cancer by carbon 11-choline positron emission tomography/computed tomography
Date of disclosure of the study information 2017/10/29
Last modified on 2023/04/26 14:06:34

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Basic information

Public title

Diagnosis of prostate cancer by carbon 11-choline positron emission tomography/computed tomography

Acronym

Choline PET/CT for prostate cancer

Scientific Title

Diagnosis of prostate cancer by carbon 11-choline positron emission tomography/computed tomography

Scientific Title:Acronym

Choline PET/CT for prostate cancer

Region

Japan


Condition

Condition

Prostate cancer

Classification by specialty

Urology Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate sensitivity and specificity of choline PET/CT for prostate cancer in several clinical stages (clinical settings), comparing with conventional imaging modalities

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

sensitivity and specificity

Key secondary outcomes



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

20 years-old <=

Age-upper limit

90 years-old >

Gender

Male

Key inclusion criteria

Cases with prostate cancer which is confirmed histologically
Cases in which prostate cancer is highly suspected clinically

Key exclusion criteria

Cases with severe liver dysfunction and/or renal dysfunction

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Atsuko Takahashi

Organization

National center for global health and medicine

Division name

Urology

Zip code


Address

Toyama 1-21-1, Shinjuku-ku, Tokyo

TEL

03-3202-7181

Email

tatsuko@hosp.ncgm.go.jp


Public contact

Name of contact person

1st name
Middle name
Last name Atsuko Takahashi

Organization

National center for global health and medicine

Division name

Urology

Zip code


Address

Toyama 1-21-1, Shinjuku-ku, Tokyo

TEL

03-3202-7181

Homepage URL


Email

panchoatsuko@yahoo.co.jp


Sponsor or person

Institute

National center for global health and medicine

Institute

Department

Personal name



Funding Source

Organization

National center for global health and medicine

Organization

Division

Category of Funding Organization

Other

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

2017 Year 10 Month 29 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 11 Month 01 Day

Date of IRB

2018 Year 03 Month 31 Day

Anticipated trial start date

2015 Year 11 Month 01 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Lesions detected by choline PET/CT will be re-evaluated by conventional imagin modalities including CT scan and bone scintigram.


Management information

Registered date

2017 Year 10 Month 29 Day

Last modified on

2023 Year 04 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033989


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name