UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000024820
Receipt number R000028564
Scientific Title Adverse events associated with ERCP for biliary diseases; a prospective multicenter observational study.
Date of disclosure of the study information 2016/11/24
Last modified on 2022/11/20 17:38:42

* 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

Adverse events associated with ERCP for biliary diseases; a prospective multicenter observational study.

Acronym

Adverse events associated with ERCP for biliary diseases.

Scientific Title

Adverse events associated with ERCP for biliary diseases; a prospective multicenter observational study.

Scientific Title:Acronym

Adverse events associated with ERCP for biliary diseases.

Region

Japan


Condition

Condition

Adverse events associated with ERCP

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To research clinical questions about adverse events associated with ERCP for biliary diseases.

Basic objectives2

Others

Basic objectives -Others

To detect risk factors.
To develop a clinical prediction rule.
To evaluate prophylactic procedures.

Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Incidence and severity of adverse events associated with ERCP.

Key secondary outcomes

1)Risk factors for post-ERCP pancreatitis.
2)Effectiveness of preventive procedures for post-ERCP pancreatitis.


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

1) Patients who underwent transpapillary ERCP for biliary diseases.
2) Patients with intact papilla.
3) Patients without history of pancreatic surgery.

Key exclusion criteria

1) Patients with clinical evidence of acute pancreatitis at the time of the procedure.
2) Patients with altered gastrointestinal anatomy. e.g. Roux-en-Y reconstruction.
3) Patients whose ASA performance status is more than 3.

Target sample size

3000


Research contact person

Name of lead principal investigator

1st name Shujiro
Middle name
Last name Yazumi

Organization

The Tazuke Kofukai Medical Research Institute Kitano Hospital

Division name

Department of Gastroenterology and Hepatology

Zip code

530-8480

Address

2-4-20, Ohgimachi, Kita-ku, Osaka, Japan 530-8480

TEL

06-6312-1221

Email

s-yazumi@kitano-hp.or.jp


Public contact

Name of contact person

1st name Shujiro
Middle name
Last name Yazumi

Organization

The Tazuke Kofukai Medical Research Institute Kitano Hospital

Division name

Department of Gastroenterology and Hepatology

Zip code

530-8480

Address

2-4-20, Ohgimachi, Kita-ku, Osaka, Japan 530-8480

TEL

06-6312-1221

Homepage URL


Email

s-yazumi@kitano-hp.or.jp


Sponsor or person

Institute

Bilio-Pancreatic Stenting study group

Institute

Department

Personal name



Funding Source

Organization

None

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

Institutional Review Board, Kitano Hospital

Address

2-4-20, Ohgimachi, Kita-ku, Osaka, Japan 530-8480

Tel

06-6312-1221

Email

rinshou@kitano-hp.or.jp


Secondary IDs

Secondary IDs

NO

Study ID_1

P16-11-006

Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

愛仁会高槻病院(大阪府)、愛仁会千船病院(大阪府)、大阪医科大学附属病院(大阪府)、大阪市立総合医療センター(大阪府)、大阪赤十字病院(大阪府)、大阪府済生会中津病院(大阪府)、大阪府立成人病センター(大阪府)、北野病院(大阪府)、北播磨総合医療センター(兵庫県)、京都大学医学附属病院(京都府)、京都府立医科大学附属病院(京都府)、近畿大学医学部附属病院(大阪府)、神戸市立医療センター西市民病院(兵庫県)、神戸大学医学部附属病院(兵庫県)、市立豊中病院(大阪府)、天理よろづ相談所病院(奈良県)、奈良県立医科大学附属病院(奈良県)、日本赤十字社和歌山医療センター(和歌山県)、ベルランド総合病院(大阪府)、淀川キリスト教病院(大阪府)、和歌山県立医科大学附属病院(和歌山県)、岡山大学病院(岡山県)、JA尾道総合病院(広島県)、川崎医科大学附属総合医療センター(岡山県)、広島市立広島市民病院(広島県)、広島赤十字・原爆病院(広島県)、島根大学医学部附属病院(島根県)、鳥取赤十字病院(鳥取県)、鳥取大学医学部附属病院(鳥取県)、松江赤十字病院(島根県)、愛媛大学附属病院(愛媛県)、香川大学医学部附属病院(香川県)、四国がんセンター(愛媛県)、大分三愛メディカルセンター(大分県)、新別府病院(大分県)、福岡大学筑紫病院(福岡県)


Other administrative information

Date of disclosure of the study information

2016 Year 11 Month 24 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

3739

Results


Results date posted


Results Delayed

Delay expected

Results Delay Reason

We are currently analyzing data.

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

Main results already published

Date of protocol fixation

2016 Year 11 Month 14 Day

Date of IRB

2016 Year 11 Month 22 Day

Anticipated trial start date

2017 Year 04 Month 01 Day

Last follow-up date

2018 Year 04 Month 30 Day

Date of closure to data entry

2018 Year 11 Month 30 Day

Date trial data considered complete

2019 Year 12 Month 02 Day

Date analysis concluded

2024 Year 03 Month 31 Day


Other

Other related information

1) Incidence and severity of adverse events associated with ERCP.
2) Relationship between pancreatic contrast injection/guidewire insertion for pancreatic duct and post-ERCP pancreatitis (PEP).
3) Relationship between difficult cannulation and PEP.
4) Relationship between precut/EST/EPBD/EPLBD and PEP.
5) Detection of risk factors for post-ERCP pancreatitis.
6) Development of clinical prediction rule for PEP.
7) Effectiveness of prophylactic pancreatic stenting.
8) Quality indicators for biliary ERCP
9) Relationship between shape of papilla and biliary cannulation and adverse events


Management information

Registered date

2016 Year 11 Month 14 Day

Last modified on

2022 Year 11 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028564


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name