UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016358
Receipt number R000018996
Scientific Title The diagnosis of pleuroperitoneal communication by contrast enhanced ultrasonography with perflubutane
Date of disclosure of the study information 2015/01/28
Last modified on 2022/02/03 02:15:30

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Basic information

Public title

The diagnosis of pleuroperitoneal communication by contrast enhanced ultrasonography with perflubutane

Acronym

The diagnosis of pleuroperitoneal communication by contrast enhanced ultrasonography with perflubutane

Scientific Title

The diagnosis of pleuroperitoneal communication by contrast enhanced ultrasonography with perflubutane

Scientific Title:Acronym

The diagnosis of pleuroperitoneal communication by contrast enhanced ultrasonography with perflubutane

Region

Japan


Condition

Condition

hydrothorax

Classification by specialty

Hepato-biliary-pancreatic medicine Chest surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The efficacy of contrast enhanced ultrasonography for the diagnosis of pleuroperitoneal communication

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The assessment of the diagnostic rate of pleuroperitonal communication by contrast enhanced ultrasonography

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 and Female

Key inclusion criteria

patients with hydrothorax and ascites

Key exclusion criteria

patients with egg allergy

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Masahiko
Middle name
Last name Koda

Organization

Tottori University, School of Medicine

Division name

Division of Medicine and Clinical Science, Department of Multidisciplinary Internal Medicine,

Zip code

683-8504

Address

Yonago 683-8504, Japan

TEL

0859-38-6527

Email

masakoda89@yahoo.co.jp


Public contact

Name of contact person

1st name Masahiko
Middle name
Last name Koda

Organization

Tottori University, School of Medicine

Division name

Division of Medicine and Clinical Science, Department of Multidisciplinary Internal Medicine,

Zip code

683-8504

Address

Yonago 683-8504, Japan

TEL

0859-38-6527

Homepage URL


Email

masakoda89@yahoo.co.jp


Sponsor or person

Institute

Tottori University, School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Tottori University, School of Medicine

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Tottori University, School of Medicine


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tottori university

Address

Yonago 683-8504, Japan

Tel

0859-38-6527

Email

masakoda89@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

2015 Year 01 Month 28 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

2015 Year 01 Month 28 Day

Date of IRB


Anticipated trial start date

2015 Year 01 Month 28 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

We investiga te the detection rate of pleuroperitoneal communication in patients with hydrothorax.

We investigate the disappearance rate of hydrothorax after the treatment of pleuroperitoneal communication.


Management information

Registered date

2015 Year 01 Month 28 Day

Last modified on

2022 Year 02 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018996


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name