UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013516
Receipt number R000014937
Scientific Title A validation study for simplified criteria of NBI magnifying endoscopy for superficial esophageal squamous cell carcinoma (SCC)
Date of disclosure of the study information 2014/04/01
Last modified on 2015/11/09 21:19:48

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Basic information

Public title

A validation study for simplified criteria of NBI magnifying endoscopy for superficial esophageal squamous cell carcinoma (SCC)

Acronym

Simplefied criteria study

Scientific Title

A validation study for simplified criteria of NBI magnifying endoscopy for superficial esophageal squamous cell carcinoma (SCC)

Scientific Title:Acronym

Simplefied criteria study

Region

Japan


Condition

Condition

superficial esophageal SCC

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Validation study for the newly simplified criteria of NBI magnifying endoscopy for superficial esophageal squamous cell neoplasms

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sensitivities of white light endoscopy and NBI magnifying endoscopy based on newly simplified criteria for superficial esophageal SCC

Key secondary outcomes

#Diagnostic yields of superficial esophageal SCC based on newly simplified criteria
#Comparison of diagnostic yields for superficial esophageal SCC based on between newly simplified criteria and conventional criteria
#Diagnostic yields of superficial esophageal SCC based on newly simplified criteria depending on status of lugol staining
#Evaluation of histopathological characteristics of superficial esophageal SCCs which were overlooked by NBI magnifying endoscopy


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are 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

NBI magnifying endoscopy

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 present or past history of SCC in the head and neck or esophagus.

The patients who agree with the informed consent

Key exclusion criteria

1.The patients who have preexisting serious disease
2.The patients who have history of radiotherapy for esophageal cancer
3.The patients who have already take chemotherapy
4.The patients who take antithrombotic drug
5.The patients who are evaluated inappropriate for the research

Target sample size

170


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Akira Dobashi

Organization

The Jikei University School of Medicine

Division name

Department of Endoscopy

Zip code


Address

3-25-8 Nishi-shimbashi, Minato-ku, Tokyo

TEL

03-3433-1111

Email

ad99061@jikei.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Akira Dobashi

Organization

The Jikei University School of Medicine

Division name

Department of Endoscopy

Zip code


Address

3-25-8 Nishi-shimbashi, Minato-ku, Tokyo

TEL

03-3433-1111

Homepage URL


Email

ad99061@jikei.ac.jp


Sponsor or person

Institute

The Jikei University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Research fund of The Jikei University School of Medicine, Department of Endoscopy

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


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

東京慈恵会医科大学附属病院(東京都)


Other administrative information

Date of disclosure of the study information

2014 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

Completed

Date of protocol fixation

2013 Year 12 Month 09 Day

Date of IRB


Anticipated trial start date

2014 Year 04 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 03 Month 26 Day

Last modified on

2015 Year 11 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014937


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name