UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006916
Receipt number R000008174
Scientific Title slow specific oral torerance induction of wheat allergy
Date of disclosure of the study information 2011/12/20
Last modified on 2023/11/30 19:19:53

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Basic information

Public title

slow specific oral torerance induction of wheat allergy

Acronym

slow specific oral torerance induction of wheat allergy

Scientific Title

slow specific oral torerance induction of wheat allergy

Scientific Title:Acronym

slow specific oral torerance induction of wheat allergy

Region

Japan


Condition

Condition

wheat allergy

Classification by specialty

Pediatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We evaluated effectiveness of frequency of wheat intake of oral specific tolerance tolerance induction of wheat

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

We avaluated the threshold level of wheat after 6month.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

the patients who intake wheat product more than 6times a week

Interventions/Control_2

the patient who intake wheat product twice a week

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

0 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

wheat allergy
the patients who can intake more than 0.5g of wheat product

Key exclusion criteria

severe wheat allergy
the patients who can not intake 0.5g of wheat

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name yuri takaoka

Organization

Osaka Prefectual Hospital Organization Osaka Prefectural medical center

Division name

pediatrics

Zip code


Address

3-7-1 Habikino city Osaka

TEL

072-957-2121

Email

takaokayu@ra.opho.jp


Public contact

Name of contact person

1st name
Middle name
Last name yuri takaoka

Organization

Osaka Prefectual Hospital Organization Osaka Prefectural medical center

Division name

pediatrics

Zip code


Address

3-7-1 Habikino city Osaka

TEL

072-957-2121

Homepage URL


Email

takaokayu@ra.opho.jp


Sponsor or person

Institute

Osaka Prefectual Hospital Organization Osaka Prefectural medical center

Institute

Department

Personal name



Funding Source

Organization

Osaka Prefectual Hospital Organization Osaka Prefectural medical center

Organization

Division

Category of Funding Organization

Local Government

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 12 Month 20 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

2011 Year 02 Month 01 Day

Date of IRB

2011 Year 01 Month 20 Day

Anticipated trial start date

2011 Year 02 Month 01 Day

Last follow-up date

2016 Year 12 Month 20 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2011 Year 12 Month 20 Day

Last modified on

2023 Year 11 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008174


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name