UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000047432
Receipt number R000054086
Scientific Title A multicenter randomized control trial comparing the resecion depth of underwater endoscopic resection and conventional endoscopic resection for colorectal tumors
Date of disclosure of the study information 2022/05/09
Last modified on 2022/10/06 12:24:53

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Basic information

Public title

A multicenter randomized control trial comparing the resecion depth of underwater endoscopic resection and conventional endoscopic resection for colorectal tumors

Acronym

RCT comparing the resecion depth of UEMR and EMR for colorectal tumors

Scientific Title

A multicenter randomized control trial comparing the resecion depth of underwater endoscopic resection and conventional endoscopic resection for colorectal tumors

Scientific Title:Acronym

RCT comparing the resecion depth of UEMR and EMR for colorectal tumors

Region

Japan


Condition

Condition

Colorectal tumors 10mm - 20mm in diameter

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safety and efficacy of UEMR for 10-20 mm colorectal tumors in comparison with those of conventional EMR

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Resection depth

Key secondary outcomes

The proportion of the presence of the muscularis mucosa, en bloc resection rate, complete resection rate, curative resection rate, resection time, adverse events, the local recurrence rate one year after


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Group A: EMR group

Interventions/Control_2

Group B: UEMR group

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

1. Colorectal tumor 10 - 20 mm in diameter
2. Aged 20 to 90 years old.
3. PS (ECOG) performance status of 0,1or2.
4. Without regard to gender.
5. An inability to discontinue antithrombotic agents and anticoagulants (except for low dose aspirin)
6. Written informed consent

Key exclusion criteria

1. Pedunculated polyp or endospically suspected T1 cancer
2. local recurrence after endoscopic resection
3. Familial adenomatous polyposis and/or inflamatory bowel disease
4. Patients taking more than two kinds of antithrombotic drugs
5. Patients with thrombocytopenia and/or bleeding tendency
6. Women during pregnancy
7. Patients enrolled in this study
8. Unsuitable patient for clinical trial judged by clinicians

Target sample size

220


Research contact person

Name of lead principal investigator

1st name Toshio
Middle name
Last name Kuwai

Organization

National Hospital Organization Kure Medical Center and Chugoku Cancer Center

Division name

Department of Gastroenterology

Zip code

737-0023

Address

3-1 Aoyama-cho, Kure, Japan

TEL

+81-823-22-3111

Email

kuwai.toshio.ur@mail.hosp.go.jp


Public contact

Name of contact person

1st name Yuzuru
Middle name
Last name Tamaru

Organization

National Hospital Organization Kure Medical Center and Chugoku Cancer Center

Division name

Department of Gastroenterology

Zip code

737-0023

Address

3-1 Aoyama-cho, Kure, Japan

TEL

+81-823-22-3111

Homepage URL


Email

tamaru.yuzuru.vh@mail.hosp.go.jp


Sponsor or person

Institute

Department of Gastroenterology, National Hospital Organization Kure Medical Center and Chugoku Cancer Center

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

National Hospital Organization Kure Medical Center and Chugoku Cancer Center

Address

3-1 Aoyama-cho, Kure, Japan

Tel

+81-823-22-3111

Email

tamaru.yuzuru.vh@mail.hosp.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

2022 Year 05 Month 09 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

2022 Year 04 Month 07 Day

Date of IRB

2022 Year 07 Month 08 Day

Anticipated trial start date

2022 Year 08 Month 01 Day

Last follow-up date

2026 Year 07 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

2022 Year 04 Month 07 Day

Last modified on

2022 Year 10 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000054086


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name