UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000043183
Receipt number R000049287
Scientific Title Confirmatory study of Simultaneous Double Stenting Using Endoscopic Ultrasound-hepaticogastrostomy in Combined Gastric Outlet and Biliary Obstructions
Date of disclosure of the study information 2021/03/01
Last modified on 2021/07/31 15:38:35

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Basic information

Public title

A Study on Optimal Biliary Drainage and Improvement of Gastrointestinal Dyspepsia in Patients with Simultaneous Biliary and Duodenal Stricture

Acronym

A Study on Optimal Biliary Drainage and Improvement of Gastrointestinal Dyspepsia in Patients with Simultaneous Biliary and Duodenal Stricture

Scientific Title

Confirmatory study of Simultaneous Double Stenting Using Endoscopic Ultrasound-hepaticogastrostomy in Combined Gastric Outlet and Biliary Obstructions

Scientific Title:Acronym

SPIRITS Study

Region

Japan


Condition

Condition

Gastric outlet obstruction and biliary obstruction

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Evaluation of clinical efficacy and safety of simultaneous EUS-HGS and endoscopic duodenal stenting for duodenal biliary stricture

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Clinical success rate

Key secondary outcomes

1) Percentage of successful clinical reduction 2) Percentage of improvement in GOO scoring system 3) Percentage of adverse events 4) Percentage of procedural success
5) Stent patency period 6) Stent survival patency period 7) Re-intervention success rate
8) Incidence of adverse events related to Re-intervention


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

Endoscopic duodenal stenting + EUS-HGS

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) Patients with biliary stricture(MBO)and duodenal stricture(GOO)due to unresectable malignancy.
2) Diagnosis of pancreatic cancer or cholangiocarcinoma by diagnostic imaging or cytological/histological diagnosis.
3) Patients must meet one of the following criteria, or in blood tests.
4) T-Bil >1.5mg/dL, 2) AST >100U/L, 3) ALT >100U/L
5) Duodenal stent is not implanted.
6) GOOSS is 0 or 1 point.
7) The location of the duodenal stricture is type.1 or type.2.
8) MBO precedes and the need for treatment of GOO arises later, and the biliary tract is reoccluded at the time of the appearance of GOO, and the need for treatment of MBO and GOO arises simultaneously.
9) When MBO and the need for treatment of GOO occur simultaneously.
10) The patient does not have Bismuth II or higher hilar bile duct stenosis.
11) There is no gastrointestinal obstruction in the small or large intestine anterior to the duodenum.
12) The patient is expected to improve with biliary drainage.
13) The patient does not have ascites of more than moderate degree.
14) P.S. (ECOG): 0, 1, 2
15) Age: 20 years or older
16) Written consent for participation in the study has been obtained from the patient.

Key exclusion criteria

1) The physician judges that enrollment in this study is inappropriate.
2) The patient has moderate or severe acute cholangitis (diagnostic criteria and severity are in accordance with Tokyo Guidelines 2018).

Target sample size

27


Research contact person

Name of lead principal investigator

1st name Susumu
Middle name
Last name Hijioka

Organization

National Cancer Center Hospital

Division name

Department of Hepatobiliary and Pancreatic Oncology Division

Zip code

104-0045

Address

5-1-1, Tsukiji, Chuo-Ku, Tokyo, Japan

TEL

03-3542-2511

Email

shijioka@ncc.go.jp


Public contact

Name of contact person

1st name Hidetoshi
Middle name
Last name Kitamura

Organization

National Cancer Center Hospital

Division name

Department of Hepatobiliary and Pancreatic Oncology Division

Zip code

104-0045

Address

5-1-1, Tsukiji, Chuo-Ku, Tokyo, Japan

TEL

03-3542-2511

Homepage URL


Email

hidkitam@ncc.go.jp


Sponsor or person

Institute

National Cancer Center Hospital

Institute

Department

Personal name



Funding Source

Organization

National Cancer Center Hospital

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Cancer Center Hospital

Address

5-1-1, Tsukiji, Chuo-Ku, Tokyo, Japan

Tel

03-3542-2511

Email

chuo-rinrishinsa-sg@ncc.go.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

2021 Year 03 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

Open public recruiting

Date of protocol fixation

2021 Year 01 Month 14 Day

Date of IRB

2021 Year 02 Month 18 Day

Anticipated trial start date

2021 Year 04 Month 01 Day

Last follow-up date

2023 Year 10 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 01 Month 29 Day

Last modified on

2021 Year 07 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000049287


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name