UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000005395
Receipt number R000006406
Scientific Title Evaluation of mucosal healing in patients with Crohn's disease by ultrasnography under balloon enteroscopy
Date of disclosure of the study information 2011/05/01
Last modified on 2019/03/24 15:43:01

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Basic information

Public title

Evaluation of mucosal healing in patients with Crohn's disease by ultrasnography under balloon enteroscopy

Acronym

mucosal healing in CD patients by EUS-balloon enteroscopy

Scientific Title

Evaluation of mucosal healing in patients with Crohn's disease by ultrasnography under balloon enteroscopy

Scientific Title:Acronym

mucosal healing in CD patients by EUS-balloon enteroscopy

Region

Japan


Condition

Condition

Crohn's disease

Classification by specialty

Medicine in general Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Detection of enteroscopic findings of mucosal healing by balloon enteroscopy and endoscopic ultrasonography
non-reccurence rate and mucosalchanges after the evaluation of balloon enteroscopy and endoscopic ultrasonography

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

non-recurence rate after 1 year

Key secondary outcomes

non-recurence rate after 1 year
modified SES-CD after 1 and 2 year
steroid-free term


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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

mucosal healing evaluation by balloon enteroscopy and endoscopic ultrasonography

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

16 years-old <=

Age-upper limit

70 years-old >

Gender

Male and Female

Key inclusion criteria

Applicable patients for balloon enteroscopy
patients with informed consent of this study

Key exclusion criteria

Non-appicable patints for balloon enteroscopy who has dangers because of clinical signs
patients without informed consent of this study

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name SHINGO KATO

Organization

Saitama Medical Center, Saitama Medical University

Division name

Department of Gastroenterology and Hepatology

Zip code


Address

1981 Kamoda, Kawagoe City, Saitama, Japan

TEL

049-228-3564

Email

skato@saitama-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shingo Kato

Organization

Saitama Medical Center, Saitama Medical University

Division name

Department of Gastroenterology and Hepatology

Zip code


Address

1981 Kamoda, Kawagoe City, Saitama, Japan

TEL

049-228-3564

Homepage URL


Email

skato@saitama-med.ac.jp


Sponsor or person

Institute

Saitama Medical University

Institute

Department

Personal name



Funding Source

Organization

Saitama Medical University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2011 Year 05 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

16

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

Completed

Date of protocol fixation

2011 Year 05 Month 01 Day

Date of IRB


Anticipated trial start date

2011 Year 06 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2018 Year 01 Month 18 Day


Other

Other related information



Management information

Registered date

2011 Year 04 Month 07 Day

Last modified on

2019 Year 03 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006406


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name