UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040467
Receipt number R000046190
Scientific Title Efficacy and feasibility of Free loop method for mucosal defects after intraluminal surgery: a pilot study
Date of disclosure of the study information 2020/05/23
Last modified on 2020/05/20 21:38:50

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Basic information

Public title

Efficacy and feasibility of Free loop method for mucosal defects after intraluminal surgery: a pilot study

Acronym

Efficacy and feasibility of Free loop method for mucosal defects after intraluminal surgery: a pilot study

Scientific Title

Efficacy and feasibility of Free loop method for mucosal defects after intraluminal surgery: a pilot study

Scientific Title:Acronym

Efficacy and feasibility of Free loop method for mucosal defects after intraluminal surgery: a pilot study

Region

Japan


Condition

Condition

Early gastrointestinal tumors, Esophageal achalasia

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To assess the efficacy of Free loop method for for mucosal defects after endoscopic resection

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

suture-maintenance rate on the postoperative day 5

Key secondary outcomes

completeness of suturing, postoperative bleeding rate, postoperative minor bleeding rate, adverse events (excluding postoperative bleeding), suturing duration


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 closure with suture and hemoclips

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)clinically-diagnosed early gastrointestinal tumor or esophageal achalasia

2)cases which are planned to remove by ESD or planned for POEM

3) 20 years-old or more

4)informed consent obtained

Key exclusion criteria

cases in which doctors in charge regarded as unsuitable to inclusion for the current study

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Mayo
Middle name
Last name Tanabe

Organization

Showa University Koto Toyosu Hospital

Division name

Digestive Diseases Center

Zip code

135-8577

Address

5-1-38 Toyosu, Koto-ku, Tokyo, 135-8577, Japan

TEL

0362046000

Email

mayo.tanabe@gmail.com


Public contact

Name of contact person

1st name Mayo
Middle name
Last name Tanabe

Organization

Showa University Koto Toyosu Hosptital

Division name

Digestive Diseases Center

Zip code

135-8577

Address

5-1-38 Toyosu Koto-ku, Tokyo, 135-8577, Japan

TEL

0362046000

Homepage URL


Email

mayo.tanabe@gmail.com


Sponsor or person

Institute

Showa University Koto Toyosu Hospital

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

Showa University Koto Toyosu Hospital

Address

5-1-38 Toyosu Koto-ku, Tokyo, Japan

Tel

0362046361

Email

th_irb@ofc.showa-u.ac.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

2020 Year 05 Month 23 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

2020 Year 05 Month 20 Day

Date of IRB

2020 Year 05 Month 15 Day

Anticipated trial start date

2020 Year 05 Month 20 Day

Last follow-up date

2022 Year 03 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

2020 Year 05 Month 20 Day

Last modified on

2020 Year 05 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046190


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name