UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045801
Receipt number R000050963
Scientific Title A multi-institutional prospective observational study of the efficacy and safety of under-gel EMR (UGEMR) for superficial colorectal tumor
Date of disclosure of the study information 2021/10/20
Last modified on 2021/10/20 10:39:44

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Basic information

Public title

A multi-institutional prospective observational study of the efficacy and safety of under-gel EMR (UGEMR) for superficial colorectal tumor

Acronym

A multi-institutional prospective observational study of the efficacy and safety of under-gel EMR (UGEMR) for superficial colorectal tumor

Scientific Title

A multi-institutional prospective observational study of the efficacy and safety of under-gel EMR (UGEMR) for superficial colorectal tumor

Scientific Title:Acronym

A multi-institutional prospective observational study of the efficacy and safety of under-gel EMR (UGEMR) for superficial colorectal tumor

Region

Japan


Condition

Condition

superficial colorectal tumors

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and the safety of Under-gel Endoscopic Mucosal Resection(UGEMR)for colorectal tumors.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

R0 resection rate of the superficial colonic tumors.

Key secondary outcomes

The rate of conversion to Endoscopic Mucosal Resection(EMR), en bloc resection, complication.
Operation time.
Usage of the gel.


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


Not applicable

Gender

Male and Female

Key inclusion criteria

The patients with the superficical colorectal tumor indicated EMR, who received sufficient explanation and consent about this study,

Key exclusion criteria

1)Major organ failure
2)Blood clotting disorder
3)Inappropriate for this study judged by the doctor.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Naoya
Middle name
Last name Okada

Organization

Omori Red Cross Hospital

Division name

Gastroenterology

Zip code

143-8527

Address

4-30-1, Chuo, Ota-Ku, Tokyo, 143-8527, Japan

TEL

+81-3-3775-3111

Email

okdnya@gmail.com


Public contact

Name of contact person

1st name Naoya
Middle name
Last name Okada

Organization

Omori Red Cross Hospital

Division name

Gastroenterology

Zip code

143-8527

Address

4-30-1, Chuo, Ota-Ku, Tokyo, 143-8527, Japan

TEL

+81-3-3775-3111

Homepage URL


Email

okdnya@gmail.com


Sponsor or person

Institute

Omori Red Cross Hospital, Department of Gastroenterology

Institute

Department

Personal name



Funding Source

Organization

This study does not need financial support

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor

Hiratsuka City Hospital, Chigasaki Municipal Hospital

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Omori Red Cross Hospital

Address

4-30-1, Chuo, Ota-Ku, Tokyo, 143-8527, Japan

Tel

+81-3-3775-3111

Email

okdnya@gmail.com


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

大森赤十字病院(東京都)


Other administrative information

Date of disclosure of the study information

2021 Year 10 Month 20 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

Preinitiation

Date of protocol fixation

2021 Year 06 Month 01 Day

Date of IRB

2021 Year 09 Month 02 Day

Anticipated trial start date

2021 Year 10 Month 20 Day

Last follow-up date

2022 Year 10 Month 30 Day

Date of closure to data entry

2023 Year 10 Month 30 Day

Date trial data considered complete

2023 Year 10 Month 30 Day

Date analysis concluded

2023 Year 10 Month 30 Day


Other

Other related information

To evaluate the safety and efficacy of under-gel EMR (UGEMR) for superficial colorectal tumors.


Management information

Registered date

2021 Year 10 Month 20 Day

Last modified on

2021 Year 10 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050963