UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000060137
Receipt number R000068783
Scientific Title Short- and Long-Term Outcomes of Stent Types for EUS-GBD
Date of disclosure of the study information 2025/12/25
Last modified on 2025/12/19 16:43:45

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Basic information

Public title

Short- and Long-Term Outcomes of Stent Types for EUS-GBD

Acronym

Short- and Long-Term Outcomes of Stent Types for EUS-GBD

Scientific Title

Short- and Long-Term Outcomes of Stent Types for EUS-GBD

Scientific Title:Acronym

Short- and Long-Term Outcomes of Stent Types for EUS-GBD

Region

Japan


Condition

Condition

Cases of gallbladder drainage for acute cholecystitis

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and patency duration of the stent in EUS-GBD

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

To evaluate the efficacy and patency duration of the stent in EUS-GBD

Key secondary outcomes

The reason of recurrent biliary obstruction after EUS-GBD.
The effectiveness of secondary stent placement.


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

18 years-old <=

Age-upper limit

120 years-old >=

Gender

Male and Female

Key inclusion criteria

>17-years-old
EUS-GBD cases for Cholecystitis

Key exclusion criteria

Patients who have applied to withdraw consent via opt-out
The patients who are otherwise judged by the investigator to be ineligible to participate in the study.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Mitsuru
Middle name
Last name Okuno

Organization

Matsunami General Hospital

Division name

Gastroenterology

Zip code

501-6062

Address

Dendai 185-1, Kasamatsu-cho, Hashima-gun, GIFU prefecture

TEL

0583880111

Email

mkobdkl@yahoo.co.jp


Public contact

Name of contact person

1st name Mitsuru
Middle name
Last name Okuno

Organization

Matsunami General Hospital

Division name

Gastroenterology

Zip code

501-6062

Address

Dendai 185-1, Kasamatsu-cho, Hashima-gun, GIFU prefecture

TEL

0583880111

Homepage URL


Email

mkobdkl@yahoo.co.jp


Sponsor or person

Institute

other

Institute

Department

Personal name



Funding Source

Organization

none

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

Matsunami General Hospital

Address

Dendai 185-1, Kasamatsu-cho, Hashima-gun, GIFU prefecture

Tel

0583880111

Email

mkobdkl@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

2025 Year 12 Month 25 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

Open public recruiting

Date of protocol fixation

2025 Year 09 Month 13 Day

Date of IRB

2025 Year 09 Month 12 Day

Anticipated trial start date

2025 Year 09 Month 13 Day

Last follow-up date

2030 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

none


Management information

Registered date

2025 Year 12 Month 19 Day

Last modified on

2025 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=R000068783