UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036257
Receipt number R000041245
Scientific Title Efficacy and safety of water-pocket endoscopic submucosal dissection for supeficial duodenal epithelial neoplasia
Date of disclosure of the study information 2019/04/01
Last modified on 2019/07/03 08:54:21

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Basic information

Public title

Efficacy and safety of water-pocket endoscopic submucosal dissection for supeficial duodenal epithelial neoplasia

Acronym

Water-pocket endoscopic submucosal dissection for supeficial duodenal epithelial neoplasia

Scientific Title

Efficacy and safety of water-pocket endoscopic submucosal dissection for supeficial duodenal epithelial neoplasia

Scientific Title:Acronym

Water-pocket endoscopic submucosal dissection for supeficial duodenal epithelial neoplasia

Region

Japan


Condition

Condition

Patients who undergo endoscopic submucosal dissection for superficilal duodenal epithelial neoplasis

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To assess the efficacy and safety of water-pocket ESD for superficial duodenal neoplasia.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

En bloc resection

Key secondary outcomes



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

20 years-old <=

Age-upper limit

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients who will undergo duodenal ESD at our hospital and have given written informed consent to this sutdy.

Key exclusion criteria

Patients who have hematological abnormality and/or undergoing hemodialysis
Patients who have serious complications
Patients who are considered to be inappropriate for this study by doctors
Patients who have polypoid lesions and/or inflammatory bowel disease
Women who have baby and are pregnant

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Hideaki
Middle name
Last name Harada

Organization

New Tokyo Hospital

Division name

Gastroenterology

Zip code

270-2232

Address

1271 Wanagaya

TEL

0081477118700

Email

nerimaendo@hotmail.co.jp


Public contact

Name of contact person

1st name Kenji
Middle name
Last name Hayasaka

Organization

New Tokyo Hospital

Division name

Gastroenterology

Zip code

270-2232

Address

1271 Wanagaya

TEL

0081477118700

Homepage URL


Email

nerimaendo@hotmail.co.jp


Sponsor or person

Institute

New Tokyo Hospital

Institute

Department

Personal name



Funding Source

Organization

New Tokyo Hospital

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

New Tokyo Hospital

Address

1271 Wanagaya

Tel

0081477118700

Email

nerimaendo@hotmail.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

2019 Year 04 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

Enrolling by invitation

Date of protocol fixation

2019 Year 04 Month 01 Day

Date of IRB

2019 Year 03 Month 24 Day

Anticipated trial start date

2019 Year 04 Month 01 Day

Last follow-up date

2020 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

20 Patients who will undergo water-pocket ESD for superficila duodenal epithelial eoplasias to evaluate the en bloc resection rates compared to historical records.


Management information

Registered date

2019 Year 03 Month 19 Day

Last modified on

2019 Year 07 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041245


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name