UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017593
Receipt number R000020391
Scientific Title Effect of PSA decreasing of a pollen extract(Cernilton) for patients with prostate biopsy: multicenter study
Date of disclosure of the study information 2015/05/15
Last modified on 2017/12/19 10:06:01

* 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

Effect of PSA decreasing of a pollen extract(Cernilton) for patients with prostate biopsy: multicenter study

Acronym

Effect of PSA decreasing of a pollen extract(Cernilton)

Scientific Title

Effect of PSA decreasing of a pollen extract(Cernilton) for patients with prostate biopsy: multicenter study

Scientific Title:Acronym

Effect of PSA decreasing of a pollen extract(Cernilton)

Region

Japan


Condition

Condition

suspected prostate cancer

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Effect of PSA decreasing of a pollen extract(Cernilton)

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

PSA decreasing rate
cancer detection 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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Maneuver

Interventions/Control_1

prostate biopsy

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

40 years-old <=

Age-upper limit


Not applicable

Gender

Male

Key inclusion criteria

patients with first episode for prostate biopsy
patients who PSA lebel is from 4 to 20 ng/ml
patients who have no induration on digital rectal examination

Key exclusion criteria

patients who using antimicrobial agent with in 3 months
patients who using a pollen extract(Cernilton) within 1 year
patients who decide not to join this study

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shingo Yamamoto

Organization

Hyogo College of Medicine

Division name

Department of Urology

Zip code


Address

1-1 Mukogawacho, Nishinomiya, Hyogo

TEL

0798-45-6366

Email

shingoy@hyo-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yoshikazu Togo

Organization

Hyogo College of Medicine

Division name

Department of Urology

Zip code


Address

1-1 Mukogawacho, Nishinomiya, Hyogo

TEL

0798-45-6366

Homepage URL


Email

ytogo@hyo-med.ac.jp


Sponsor or person

Institute

Department of Urology,Hyogo College of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Urology,Hyogo College of Medicine

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

2015 Year 05 Month 15 Day


Related information

URL releasing protocol


Publication of results

Partially published


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

2014 Year 01 Month 01 Day

Date of IRB


Anticipated trial start date

2014 Year 01 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

2015 Year 05 Month 15 Day

Last modified on

2017 Year 12 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020391


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name