UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022495
Receipt number R000025931
Scientific Title Prospective clinical study of histological diagnostic accuracy on EUS-guided FNA using 20G FNA needle
Date of disclosure of the study information 2016/06/01
Last modified on 2017/02/10 16:50:02

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Basic information

Public title

Prospective clinical study of histological diagnostic accuracy on EUS-guided FNA using 20G FNA needle

Acronym

Diagnostic yield of 20G FNA needle on EUS-guided FNA

Scientific Title

Prospective clinical study of histological diagnostic accuracy on EUS-guided FNA using 20G FNA needle

Scientific Title:Acronym

Diagnostic yield of 20G FNA needle on EUS-guided FNA

Region

Japan


Condition

Condition

Pancreatic tumor

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Evaluate diagnostic accuracy

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Histological diagnostic accracy

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

Device,equipment

Interventions/Control_1

ProCore 20G FNA needle

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) over 20 years old
2)having pancreatic tumor
3)Performance status is under 2
4)Patients who have no serious complications
5)EUS-FNA is needed
6)Informed consent is obtained

Key exclusion criteria

1)Risk of EUS-FNA such as easy bleeding
2)Patient refuse to undergo EUS-FNA
3)other reason according to endoscopist's opinions

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takeshi Ogura

Organization

Osaka Medical College

Division name

Second Department of Internal Medicine

Zip code


Address

2-7 Daigaku-machi, Takatsuki-shi, Osaka 569-8686, Japan

TEL

0726-83-1221

Email

oguratakeshi0411@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takeshi Ogura

Organization

Osaka Medical College

Division name

Second Department of Internal Medicine

Zip code


Address

2-7 Daigaku-machi, Takatsuki-shi, Osaka 569-8686, Japan

TEL

0726-83-1221

Homepage URL


Email

oguratakeshi0411@yahoo.co.jp


Sponsor or person

Institute

Osaka Medical College

Institute

Department

Personal name



Funding Source

Organization

Osaka Medical College

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

2016 Year 06 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

Completed

Date of protocol fixation

2016 Year 05 Month 27 Day

Date of IRB


Anticipated trial start date

2016 Year 06 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

2016 Year 05 Month 27 Day

Last modified on

2017 Year 02 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025931


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name