UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000031363
Receipt number R000035813
Scientific Title Effectiveness of the full-length metallic ureteral stent for the patinet of malignant ureteral obstruction
Date of disclosure of the study information 2018/02/20
Last modified on 2020/08/24 08:38:32

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Basic information

Public title

Effectiveness of the full-length metallic ureteral stent for the patinet of malignant ureteral obstruction

Acronym

Effectiveness of the full-length metallic ureteral stent

Scientific Title

Effectiveness of the full-length metallic ureteral stent for the patinet of malignant ureteral obstruction

Scientific Title:Acronym

Effectiveness of the full-length metallic ureteral stent

Region

Japan


Condition

Condition

malignant ureteral obstruction

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To assess the effect of full-length metallic ureteral stent for the patient of malignant ureteral obstruction

Basic objectives2

Others

Basic objectives -Others

To assess the factor of full-length metallic ureteral stent obstruction

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Stent failure free survival

Key secondary outcomes

Assesment of risk factors of stent failure


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


Not applicable

Gender

Male and Female

Key inclusion criteria

1) Patients aged 20 years or older.
2) Patients with malignant ureteral obstruction

Key exclusion criteria

1) Patient with difficulty to perform transurethral treatment
2) Patients who are judged to be inappropriate.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Yasuyuki
Middle name
Last name Kobayashi

Organization

Kinki Central Hospital of Mutual Aid Association of Public Teachers

Division name

Department of Urology

Zip code

664-8533

Address

3-1 Kurumazuka, Itami, Hyogo 664-8533, Japan

TEL

072-781-3712

Email

ya_su_koba@yahoo.co.jp


Public contact

Name of contact person

1st name Yasuyuki
Middle name
Last name Kobayashi

Organization

Kinki Central Hospital of Mutual Aid Association of Public Teachers

Division name

Department of Urology

Zip code

664-8533

Address

3-1 Kurumazuka, Itami, Hyogo 664-8533, Japan

TEL

072-781-3712

Homepage URL


Email

ya_su_koba@yahoo.co.jp


Sponsor or person

Institute

Departments of Urology, Kinki Central Hospital of Mutual Aid Association of Public Teachers, Hyogo, Japan

Institute

Department

Personal name



Funding Source

Organization

Kinki Central Hospital of Mutual Aid Association of Public Teachers, Hyogo, Japan

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

Kinki Central Hospital of Mutual Aid Association of Public School Teachers

Address

3-1 Kurumazuka, Itami, Hyogo 664-8533, Japan

Tel

072-781-3712

Email

ya_su_koba@yahoo.co.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

2018 Year 02 Month 20 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

2016 Year 01 Month 18 Day

Date of IRB

2016 Year 01 Month 18 Day

Anticipated trial start date

2016 Year 04 Month 15 Day

Last follow-up date

2020 Year 01 Month 15 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

public recruiting


Management information

Registered date

2018 Year 02 Month 19 Day

Last modified on

2020 Year 08 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000035813


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name