UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037677
Receipt number R000042968
Scientific Title Study on the relationship between the breath acetaldehyde/ethanol ratio and the risk of Head and Neck/Esophageal cancer
Date of disclosure of the study information 2019/08/13
Last modified on 2022/03/18 20:55:43

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Basic information

Public title

Study on the relationship between the breath acetaldehyde/ethanol ratio and the risk of Head and Neck/Esophageal cancer

Acronym

Breath AERO-E study

Scientific Title

Study on the relationship between the breath acetaldehyde/ethanol ratio and the risk of Head and Neck/Esophageal cancer

Scientific Title:Acronym

Breath AERO-E study

Region

Japan


Condition

Condition

Esophageal cancer
Head and Neck cancer

Classification by specialty

Gastroenterology Oto-rhino-laryngology

Classification by malignancy

Malignancy

Genomic information

YES


Objectives

Narrative objectives1

This study clarifies the usefulness of the concentration ratio of acetaldehyde and ethanol calculated from exhaled gas after ingesting a small amount of ethanol as a new means of investigating the risk of head and neck / esophageal cancer.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Correlation between A/E ratio in expired air and Lugol-voiding lesions grade

Key secondary outcomes



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

1)diagnosed with head and neck cancer, esophageal cancer, gastric cancer, or suspected of having the disease, and scheduled to undergo endoscopy (iodine staining) for detailed examination and follow up after treatment
2)over 20 years old
3)clinical laboratory values meet the following standards
AST, ALT, GGTP Less than twice the facility standard upper limit of the research institution
4)obtain written consent from the subject

Key exclusion criteria

1)allergic to alcohol
2)allergic to iodine
3)pregnant or may be pregnant or breastfeeding
4)serious complications (such as chronic obstructive pulmonary disease that requires oxygen inhalation, pulmonary fibrosis, symptomatic heart failure)
5)history of bronchial asthma, drug allergies, etc.
6)history of cancer treatment other than endoscopic treatment
7)history of resection of the esophagus, stomach, liver, pancreas (excluding endoscopic treatment)
8)stricture in esophagus
9)judged inappropriate by the attending physician

Target sample size

360


Research contact person

Name of lead principal investigator

1st name Manabu
Middle name
Last name Muto

Organization

Kyoto University Hospital

Division name

Department of Clinical Oncology

Zip code

606-8507

Address

54kawahara-cho, shogoin, sakyo-ku, Kyoto

TEL

075-751-4592

Email

mmuto@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name Yuki
Middle name
Last name Kondo

Organization

Graduate school of Medicine, Kyoto University

Division name

Department of Therapeutic Oncology

Zip code

606-8507

Address

54kawahara-cho, shogoin, sakyo-ku, Kyoto

TEL

075-751-4592

Homepage URL


Email

ykondo@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Kyoto University

Institute

Department

Personal name



Funding Source

Organization

KUBIX Inc.
Nissha Co.,Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kyoto University Graduate school and Faculty of Medicine, Kyoto University Hospital, Ethics Committe

Address

yoshidakonoecho, sakyoku, kyoto city

Tel

075-753-4680

Email

ethcom@kuhp.kyoto-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

2019 Year 08 Month 13 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

Enrolling by invitation

Date of protocol fixation

2019 Year 08 Month 13 Day

Date of IRB

2019 Year 11 Month 26 Day

Anticipated trial start date

2019 Year 10 Month 13 Day

Last follow-up date

2022 Year 11 Month 26 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Observation items
1)Alcohol, tobacco and meal questionnaire
2)Genetic testing
3)Breath gas test
4)Endoscopic image


Management information

Registered date

2019 Year 08 Month 13 Day

Last modified on

2022 Year 03 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042968


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name