UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036663
Receipt number R000041771
Scientific Title Prospective study of low dose rate brachytherapy combined with stereotactic body radiotherapy for very-high risk prostate cancer
Date of disclosure of the study information 2019/07/01
Last modified on 2022/05/09 09:19:18

* 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

Prospective study of low dose rate brachytherapy combined with stereotactic body radiotherapy for very-high risk prostate cancer

Acronym

Prospective study of low dose rate brachytherapy combined with stereotactic body radiotherapy for very-high risk prostate cancer

Scientific Title

Prospective study of low dose rate brachytherapy combined with stereotactic body radiotherapy for very-high risk prostate cancer

Scientific Title:Acronym

Prospective study of low dose rate brachytherapy combined with stereotactic body radiotherapy for very-high risk prostate cancer

Region

Japan


Condition

Condition

prostate cancer

Classification by specialty

Urology Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To examine the safety and effectiveness of low dose rate brachytherapy combined with stereotactic body radiotherapy for very-high risk prostate cancer

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

3-year actuarial Grade 3 toxicity rate

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

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

radiotherapy

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

80 years-old >

Gender

Male

Key inclusion criteria

1) pathologically confirmed adenocarcinoma
2) >=T3b or Gleason socre >=9
3) performance status >=1

Key exclusion criteria

1) active tumor in other organs
2) uncontrolled diabetes
3) Severe concomitant diseases
4) psychiatric disease
5) history of pelvic irradiation
6) history of chemotherapy
7) physician's estimation

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Hiromichi
Middle name
Last name Ishiyama

Organization

Kitasato University school of medicine

Division name

Department of Radiation Oncology

Zip code

252-0374

Address

1-15-1 kitasato, satamiharashi minamiku,kanagawa,Japan

TEL

042-778-8453

Email

hishiyam@kitasato-u.ac.jp


Public contact

Name of contact person

1st name Hiromichi
Middle name
Last name Ishiyama

Organization

Kitasato university school of medicine

Division name

Department of radiation oncology

Zip code

252-0374

Address

1-15-1 kitasato, sagamiharashi minamiku, kanagawa, japan

TEL

042-778-8453

Homepage URL


Email

hishiyam@kitasato-u.ac.jp


Sponsor or person

Institute

Kitasato university

Institute

Department

Personal name



Funding Source

Organization

kitasato univeristy

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

Kitasato university

Address

1-15-1 kitasato, sagamiharashi minamiku, kanagawa, japan

Tel

042-778-8453

Email

hishiyam@kitasato-u.ac.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

2019 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

Enrolling by invitation

Date of protocol fixation

2019 Year 07 Month 01 Day

Date of IRB

2019 Year 08 Month 07 Day

Anticipated trial start date

2019 Year 08 Month 07 Day

Last follow-up date

2026 Year 05 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

2019 Year 05 Month 07 Day

Last modified on

2022 Year 05 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041771


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name