UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027117
Receipt number R000031073
Scientific Title The influence of a peritoneovenous shunt for intractable ascites on renal function
Date of disclosure of the study information 2017/06/01
Last modified on 2018/10/30 20:16:48

* 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

The influence of a peritoneovenous shunt for intractable ascites on renal function

Acronym

The influence of a peritoneovenous shunt on renal function

Scientific Title

The influence of a peritoneovenous shunt for intractable ascites on renal function

Scientific Title:Acronym

The influence of a peritoneovenous shunt on renal function

Region

Japan


Condition

Condition

intractable ascites

Classification by specialty

Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the relationship between PVS and renal function

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Changes in eGFR before, 1 day after, and 1 week after PVS placement

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

15 years-old <=

Age-upper limit

85 years-old >=

Gender

Male and Female

Key inclusion criteria

1)ascites that could not be managed by repeated abdominal paracentesis and/or diuretic therapy
2) ascites that induced deterioration in QOL

Key exclusion criteria

1)severe heart failure
2)ascites with infection or mucinous component

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kenichi Kato

Organization

Iwate Medical University

Division name

Department of Radiology

Zip code


Address

19-1 Uchimaru, Morioka

TEL

019-651-5111

Email

kkato@iwate-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takafumi Segawa

Organization

Iwate Medical University

Division name

Department of Radiology

Zip code


Address

19-1 Uchimaru, Morioka

TEL

019-651-5111

Homepage URL


Email

lendido-el@hotmail.co.jp


Sponsor or person

Institute

Iwate Medical University

Institute

Department

Personal name



Funding Source

Organization

Iwate Medical University

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


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 06 Month 01 Day


Related information

URL releasing protocol


Publication of results

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

2017 Year 04 Month 20 Day

Date of IRB


Anticipated trial start date

2017 Year 05 Month 10 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2017 Year 10 Month 31 Day


Other

Other related information

Not particular


Management information

Registered date

2017 Year 04 Month 24 Day

Last modified on

2018 Year 10 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031073


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name