UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000025656
Receipt number R000029512
Scientific Title Endoscopic biliary drainage for postoperative anastomotic stricture
Date of disclosure of the study information 2017/01/12
Last modified on 2023/07/20 15:38:50

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Basic information

Public title

Endoscopic biliary drainage for postoperative anastomotic stricture

Acronym

EBD for postoperative anastomotic stricture

Scientific Title

Endoscopic biliary drainage for postoperative anastomotic stricture

Scientific Title:Acronym

EBD for postoperative anastomotic stricture

Region

Japan


Condition

Condition

Postoperative anastomotic biliary stricture

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safety and efficacy of temporary placement of fully covered self-expandable metal stents (FCSEMSs) to treat postoperative anastomotic stricture

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Safety

Key secondary outcomes

Efficacy


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

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Temporary placement of fully covered self-expandable metal stents (FCSEMSs) to treat postoperative anastomotic stricture

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. Maintained major organ function marrow, heart, liver,
lungs, and kidneys. Absence of heart failure, platelet counts
2. Performance status (Eastern Cooperative Oncology Group):
0, 1, 2, or 3.
3.Anastomosis stricture without tumor
4.Wituout gastrointestinal obstruction
5.Without severe ascites
6.Predicted survival within 1 month.
7.Informed consent provided by the patient.

Key exclusion criteria

1.Pregnancy.
2.The case that the attending phycisian judged inappropriate

Target sample size

15


Research contact person

Name of lead principal investigator

1st name Kazuo
Middle name
Last name Hara

Organization

Aichi Cancer Center Hospital

Division name

Gastroenterology

Zip code

4648681

Address

1-1 Kanokoden, Chikusa-ku, Nagoya, Aichi 464-8681, Japan

TEL

0527626111

Email

khara@aichi-cc.jp


Public contact

Name of contact person

1st name Nozomi
Middle name
Last name Okuno

Organization

Aichi Cancer Center Hospital

Division name

Gastroenterology

Zip code

4648681

Address

1-1, kanokoden, chikusa-ku,Nagoya

TEL

0527626111

Homepage URL


Email

nokuno@aichi-cc.jp


Sponsor or person

Institute

Aichi Cancer Center Hospital

Institute

Department

Personal name



Funding Source

Organization

Aichi Cancer Center Hospital

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

Aichi Cancer Center Hospital

Address

1-1, kanokoden, chikusa-ku,Nagoya

Tel

0527626111

Email

irb@aichi-cc.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

2017 Year 01 Month 12 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

No longer recruiting

Date of protocol fixation

2017 Year 01 Month 12 Day

Date of IRB

2017 Year 01 Month 12 Day

Anticipated trial start date

2017 Year 01 Month 13 Day

Last follow-up date

2023 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 01 Month 12 Day

Last modified on

2023 Year 07 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029512


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name