UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000053662
Receipt number R000061245
Scientific Title Development of blood circulation quantification method using small number of frame data in dynamic contrast-enhanced MRI of prostate cancer
Date of disclosure of the study information 2024/03/01
Last modified on 2024/08/21 15:34:02

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Development of blood circulation quantification method using small number of frame data in dynamic contrast-enhanced MRI of prostate cancer

Acronym

Quantification of blood circulation for small number frame data in prostate DCE-MRI

Scientific Title

Development of blood circulation quantification method using small number of frame data in dynamic contrast-enhanced MRI of prostate cancer

Scientific Title:Acronym

Quantification of blood circulation for small number frame data in prostate DCE-MRI

Region

Japan


Condition

Condition

Prostate cancer

Classification by specialty

Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to develop a method to precisely quantify blood circulation using a small number of frame data obtained from low temporal resolution or short length scans in dynamic contrast-enhanced MRI of prostate cancer.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Validity of blood circulation parameters derived from data with frame number reduction

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


Not applicable

Age-upper limit


Not applicable

Gender

Male

Key inclusion criteria

Patients who underwent dynamic contrast-enhanced, T2-weighted, and diffusion-weighted prostate MRI at our institution between March 2013 and November 2023.

Key exclusion criteria

Patients who refused secondary use of information at the time of informed consent
Patients who requested that their information not be used during the opt-out period

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Takayuki
Middle name
Last name Obata

Organization

National Institutes for Quantum Science and Technology

Division name

Department of Molecular Imaging and Theranostics

Zip code

263-8555

Address

4-9-1, Anagawa, Inage-ku, Chiba

TEL

043-206-3230

Email

obata.takayuki@qst.go.jp


Public contact

Name of contact person

1st name Takayuki
Middle name
Last name Obata

Organization

National Institutes for Quantum Science and Technology

Division name

Department of Molecular Imaging and Theranostics

Zip code

263-8555

Address

4-9-1, Anagawa, Inage-ku, Chiba

TEL

043-206-3230

Homepage URL


Email

obata.takayuki@qst.go.jp


Sponsor or person

Institute

National Institutes for Quantum Science and Technology

Institute

Department

Personal name



Funding Source

Organization

National Institutes for Quantum Science and Technology

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

National Institutes for Quantum Science and Technology, Certified Review Board

Address

4-9-1, Anagawa, Inage-ku, Chiba

Tel

043-206-4709

Email

helsinki@qst.go.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



Other administrative information

Date of disclosure of the study information

2024 Year 03 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

40

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

No longer recruiting

Date of protocol fixation

2024 Year 02 Month 14 Day

Date of IRB

2024 Year 02 Month 14 Day

Anticipated trial start date

2024 Year 03 Month 01 Day

Last follow-up date

2024 Year 05 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This is a retrospective study.


Management information

Registered date

2024 Year 02 Month 20 Day

Last modified on

2024 Year 08 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061245