UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019561
Receipt number R000022513
Scientific Title The analysis of urinary eicosanoids in patients with controlled aspirin exacerbated respiratory disease (AERD)
Date of disclosure of the study information 2015/11/02
Last modified on 2021/11/02 09:16:37

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Basic information

Public title

The analysis of urinary eicosanoids in patients with controlled aspirin exacerbated respiratory disease (AERD)

Acronym

The analysis of urinary eicosanoids in patients with controlled AERD

Scientific Title

The analysis of urinary eicosanoids in patients with controlled aspirin exacerbated respiratory disease (AERD)

Scientific Title:Acronym

The analysis of urinary eicosanoids in patients with controlled AERD

Region

Japan


Condition

Condition

Aspirin exacerbated respiratory disease (AERD)

Classification by specialty

Pneumology Clinical immunology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To search the eicosanoids relevant to AERD

Basic objectives2

Others

Basic objectives -Others

diagnosis of pathologic conditions

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Differences in eicosanoids between AERD and non-AERD

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

80 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Patients diagnosed with AERD or non-AERD by a systemic aspirin provocation test within the last fifteen years
2)Patients evaluated as controlled asthma

Key exclusion criteria

Patients considered unsuitable by the attending physician

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Masami
Middle name
Last name Taniguchi

Organization

Sagamihara National Hospital

Division name

Clinical Research Center for Allergy and Rheumatology

Zip code

2520392

Address

18-1 Sakuradai Minami-ku Sagamihara Kanagawa Japan

TEL

042-742-8311

Email

taniguchi.masami.ne@mail.hosp.go.jp


Public contact

Name of contact person

1st name Yosuke
Middle name
Last name Kamide

Organization

Sagamihara National Hospital

Division name

Clinical Research Center for Allergy and Rheumatology

Zip code

2520392

Address

18-1 Sakuradai Minami-ku Sagamihara Kanagawa Japan

TEL

042-742-8311

Homepage URL


Email

m08702012@gunma-u.ac.jp


Sponsor or person

Institute

Sagamihara National Hospital

Institute

Department

Personal name



Funding Source

Organization

Labour Sciences Research Grant

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Hospital Organization Sagamihara National Hospital

Address

18-1 Sakuradai Minami-ku Sagamihara Kanagawa Japan

Tel

042-742-8311

Email

sugawara.rumi.rz@mail.hosp.go.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

2015 Year 11 Month 02 Day


Related information

URL releasing protocol

Currently being analyzed

Publication of results

Unpublished


Result

URL related to results and publications

Currently being analyzed

Number of participants that the trial has enrolled

141

Results

Currently being analyzed

Results date posted

2021 Year 11 Month 02 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

Currently being analyzed

Participant flow

Currently being analyzed

Adverse events

no

Outcome measures

Currently being analyzed

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

No longer recruiting

Date of protocol fixation

2015 Year 09 Month 15 Day

Date of IRB

2015 Year 09 Month 15 Day

Anticipated trial start date

2015 Year 10 Month 22 Day

Last follow-up date

2020 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Study design: case-control study
Subjects:All subjects that our hospital visited by broncholial asthma, and met the selection criteria.
Analyzing items: background factor (age, sex, coexisting disease, etc), subjective and objective symptom, urinary eicosanoids, lung function test, blood examination (IgE, RAST).


Management information

Registered date

2015 Year 10 Month 29 Day

Last modified on

2021 Year 11 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022513


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name