UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000026710
Receipt number R000030663
Scientific Title MRI/TRUS fusion target biopsy against prostate cancer using real-time virtual sonography
Date of disclosure of the study information 2017/03/27
Last modified on 2017/03/26 20:43:49

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Basic information

Public title

MRI/TRUS fusion target biopsy against prostate cancer using real-time virtual sonography

Acronym

RVS fusion target biopsy against prostate cancer

Scientific Title

MRI/TRUS fusion target biopsy against prostate cancer using real-time virtual sonography

Scientific Title:Acronym

RVS fusion target biopsy against prostate cancer

Region

Japan


Condition

Condition

Prostate cancer

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To examine the efficacy and efficiency of the prostate biopsy using real-time virtual sonography against patients suspicious of prostate cancer compared to systematic biopsy

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Cancer-detected rates of the targeted biopsy compared to systematic biopsy

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

Real-time virtual sonography (target biopsy)

Interventions/Control_2

systematic biopsy

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

40 years-old <=

Age-upper limit

80 years-old >

Gender

Male

Key inclusion criteria

1) PSA level (2.5-20ng/ml)
2) Suspicious of localized prostate cancer by digital rectal examination
3) Suspicious of localized prostate cancer by MRI (PI-RADS score >=3)
4) patients who was obtained informed consent

Key exclusion criteria

1) Suspicious of invasive prostate cancer by digital rectal examination
2) Suspicious of invasive prostate cancer by MRI
3) Patients with coagulation disorder
4) Patients who can not be performed TRUS because of anal stenosis

Target sample size

275


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shuzo Hamamoto

Organization

Nagoya City University Graduate School of Medical Sciences

Division name

Nephro-urology

Zip code


Address

1 Kawasumi Muzuho-cho, Mizuho-Ku, Nagoya, Japan

TEL

052-853-8266

Email

hamamo10@med.nagoya-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shuzo Hamamoto

Organization

Nagoya City University Graduate School of Medical Sciences

Division name

Nephro-urology

Zip code


Address

1 Kawasumi Muzuho-cho, Mizuho-Ku, Nagoya, Japan

TEL

052-853-8266

Homepage URL


Email

hamamo10@med.nagoya-cu.ac.jp


Sponsor or person

Institute

Nagoya City University Graduate School of Medical Sciences

Institute

Department

Personal name



Funding Source

Organization

Nagoya City University Graduate School of Medical Sciences

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

2017 Year 03 Month 27 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

Open public recruiting

Date of protocol fixation

2017 Year 03 Month 26 Day

Date of IRB


Anticipated trial start date

2017 Year 03 Month 27 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

2017 Year 03 Month 26 Day

Last modified on

2017 Year 03 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030663


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name